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l-aspartic acid-beta-methyl ester hcl 4

Enantiomerically Pure Dibenzyl Esters of l

Jun 11, 2015(S)-Dibenzyl aspartate p-toluenesulfonate [(S)-1TsOH] and (S)-dibenzyl glutamate p-toluenesulfonate [(S)-2TsOH] were efficiently prepared from the respective l-amino acids and benzyl alcohol with very high yields by using cyclohexane as a water azeotroping solvent instead of benzene, carbon tetrachloride, toluene, or benzyl alcohol itself, as reported in literature methods.

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N

Nov 01, 2009The conformations of the backbone and the side-chain, however, are slightly different from those of L-aspartic acid. The torsion angles, N1–C1–C2–C3 and N1–C1–C4–O4, are found to be 62.5 (4) and 17.0 (5), respectively. For L-aspartic acid, the corresponding angles are -60.3 and

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Enantiomerically Pure Dibenzyl Esters of l

The preparation of (S)-1TsOH from L-aspartic acid, 4 equiv of benzyl alcohol, and little more than 1 equiv of p-toluenesulfonic acid inbenzene under refluxwas described in1957.21 According to such a procedure, water is azeotropically removed during the reaction

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L

L-Aspartic acid powder (pure) A highly stimulatory additive for carp, in tests it is shown that herbivorous fish prefer acidic substances like aspartic acid. It is a metabolite in the citric acid and urea cycle, participates in gluconeogenesis and acts as a neurotransmitter. It is mainly found in

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Quantitative measurement of N

Stock solutions were standardized against unlabeled NA-Asp and stored at -20 C. Sample preparation After addition of the internal standard (1 Mg per 50,ul of methanol), 100 ml of urine were acidified to pH 2.0 with 0.1 M hydrochloric acid and extracted twice with 1 ml of ethyl acetate.

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YICK

ph-1857dj 2177-63-1 l-aspartic acid beta-benzyl ester mis-24090 1791-13-5 l-aspartic acid bis(1,1-dimethylethyl) ester hydrochloride unie-10620 125229-60-9 l-aspartic acid bis-allyl ester p-toluenesulfonate salt ph-1857va 10389-09-0 21059-46-1 (unspecified ratio) l-aspartic acid calcium salt mis-22209 39162-75-9 l-aspartic acid calcium salt mis

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Aspartic Acid

Aspartic acid also known as aspartate, is an α-amino acid that is used in the biosynthesis of proteins. Similar to all other amino acids it contains an amino group and a carboxylic acid. Its α-amino group is in the protonated –NH + 3 form under physiological conditions,

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L Alanine Methyl Ester Hydrochloride Manufacturer in

We are offering l-alanine methyl ester hydrochloride. Our organization hold expertise in providing superior grade l-alanine methyl ester hydrochloride to our precious customers. Our offered l-alanine methyl ester hydrochloride is widely appreciated by our.

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L

Chemcd provide global chemical suppliers of L-ASPARTIC ACID BETA-METHYL ESTER HYDROCHLORIDE Cas#:16856-13-6,include Price,Boiling point,Melting point,L-ASPARTIC ACID BETA-METHYL ESTER HYDROCHLORIDE Cas#:16856-13-6 MSDS,Nmr,Spectrum.You can order L-ASPARTIC ACID BETA-METHYL ESTER HYDROCHLORIDE Cas#:16856-13-6 on chemcd.

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(PDF) Substrate Specificity and Reaction Mechanism of

The results are consistent with an L-asparaginase-like reaction pathway which involves a beta-aspartyl enzyme intermediate. Since glycoasparaginase is active toward a series of structurally different glycoasparagines, we suggest the revised systematic name of N4-

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Products list

L-Aspartic acid di-tert-butyl ester hydrochloride: 2886-33-1: L-Aspartic acid dibenzyl ester 4-toluenesulfonate: 132388-57-9: N-Cbz-N'-trityl-L-asparagine: 86060-99-3: 16652-71-4: L-Proline benzyl ester hydrochloride: 1738-77-8: L-Leucine benzyl ester p-toluenesulfonate salt: 87-72-9: L(+)-Arabinose: 33208-99-0: L-Alaninamide hydrochloride:

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R31558

H-Asp(OMe)-OHHCl. : H-ASP(OME)-OH HCL; ASPARTIC ACID(OME)-OH HCL; beta-Methyl L-aspartate hydrochloride; l-asparitc acid 4-methyl ester hydrochloride; L-ASPARTIC ACID B-METHYL ESTER HCL; L-ASPARTIC ACID B-METHYL ESTER HYDROCHLORIDE; L-ASPARTIC ACID BETA-METHYL ESTER HCL; L-ASPARTIC ACID BETA-METHYL ESTER HYDROCHLORIDE. CAS

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D-Aspartic Acid, beta-Methyl Ester, HCl CAS 22728-89-8 Syn: D-Aspartic Acid, 4-Methyl Ester, Hydrochloride Structure: Mol. Formula C 5 H 9 NO 4 HCl Mol. Wt. 182.63 Source Synthetic Mnft Date Lot No. Re-test Test Specification Results Identity TLC; IR Appearance White, microcrystalline solid

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d

L-Aspartic acid β-methyl ester hydrochloride | Sigma-Aldrich. Packaging 1, 25 g in poly bottle Biochem/physiol Actions L-Aspartic acid β-methyl ester is used for the organic synthesis of S-enantiomers of hanishin, longamide B, and longamide B methylester, of 1-β-methylcarbapenem, TA-949 and for the enzymatic synthesis of a CCK-4 tripeptide fragment

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US8039662B2

US8039662B2 US12/528,691 US52869108A US8039662B2 US 8039662 B2 US8039662 B2 US 8039662B2 US 52869108 A US52869108 A US 52869108A US 8039662 B2 US8039662 B2 US 8039662B2 Authority US United States Prior art keywords amino acid preferably methanol acid mixture Prior art date 2007-03-09 Legal status (The legal status is an assumption and is not a legal conclusion.

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AMINO ACIDS

L-Aspartic acid di-tert-butyl ester hydrochloride. 1791-13-5. H-Asp(OBut)-OButHCl. 1791-13-5. L-Glutamic acid γ-hydrazide. 1820-73-1. N-Trifluoroacetyl-L-methionine methyl ester. 1830-73-5. DL-Aspartic acid beta-methyl ester hydrochloride. 1835-52-5. L-2,4-Diaminobutyric acid dihydrochloride

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Swanson Ultra L

An amino acid involved in many fundamental biochemical processes, L-aspartic acid is a key player in the production of adenosine triphosphate (ATP), the fuel that powers every cell in the human body. It also supports the activity of the coenzyme NADH (nicotinamide adenine dinucleotide), which plays an important role in the neurological processes responsible for healthy memory and mental sharpness.

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Synthesis of a novel zwitterionic biodegradable poly (α,β

Aug 01, 2011A novel zwitterionic polypeptide derivative, denoted as His-PAsp/PAsp, was successfully synthesized by amidation of Poly (α,β-l-aspartic acid) with l-histidine methyl ester.Turbidity, zeta potential and 1 H NMR measurements were used to study the aggregation behaviors of His-PAsp/PAsp under different pH values. The modified polypeptide derivative composed of electro-negatively carboxylic

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beta

The L-Aspartic acid,4-methyl ester, hydrochloride (1:1) is an organic compound with the formula C 5 H 9 NO 4. HCl. The IUPAC name of this chemical is 2-amino-4-methoxy-4-oxobutanoic acid hydrochloride. With the CAS registry number 16856-13-6, it is also named as 4-Methyl hydrogen L-aspartate HCl.

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L

beta-Methyl L-aspartate hydrochloride: : H-ASP(OME)-OH HCL;ASPARTIC ACID(OME)-OH HCL;beta-Methyl L-aspartate hydrochloride;l-asparitc acid 4-methyl ester hydrochloride;L-ASPARTIC ACID B-METHYL ESTER HCL;L-ASPARTIC ACID B-METHYL ESTER HYDROCHLORIDE;L-ASPARTIC ACID BETA-METHYL ESTER HCL;L-ASPARTIC ACID BETA-METHYL ESTER HYDROCHLORIDE

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Practical Synthesis of (R)

A facile and economical synthesis of a novel orally active 1-β-methylcarbapenem, TA-949 (1), is described. The key process involves an efficient synthesis of the C-2 side chain (R)-4-mercaptopyrrolidine-2-thione 2 from l-aspartic acid and the construction of the 1-β-methylcarbapenem skeleton. The mercapto group of 2 with an R-configuration was formed via deaminative bromination of

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CA1286845C

ABSTRACT Disclosed herein is a process for preparing a-L-aspartyl-L-phenylalanine methyl ester or its hydrochloride from 5-benzyl-3,6-dioxo-2-piperazine acetic acid or its methyl ester, prepared without using L-penylalanine methyl ester which involves problems in its stability, as a raw material.

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Boc

Visit ChemicalBook To find more Boc-L-aspartic acid 4-methyl ester(59768-74-0) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. You can also browse global suppliers,vendor,prices,Price,manufacturers of Boc-L-aspartic acid 4-methyl ester(59768-74-0).

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Synthesis and rearrangements of D

Synthesis and rearrangements of D-glucosyl esters of aspartic acid linked through the 1- or 4-carboxyl group. Hydrogenolysis of 7beta under the above conditions led to intermolecular transesterification with scission of the C-1 ester bond to give 1-(2-methoxyethyl) L-aspartic acid and D-glucose. Catalytic hydrogenation of 7alpha and 7beta

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Amino Acids Derivatives

L-Aspartic Acid Diethyl Ester Hydrochloride extrapure, 98% L-Aspartic Acid Dimethyl Ester Hydrochloride extrapure, 98% L-Aspartic Acid extrapure CHR, 99% L-Citrulline extrapure CHR, 99% L-Dopa extrapure, 99% L-Glutamic Acid extrapure CHR, 99% L-Glutamic Acid Benzyl Ester extrapure, 99%

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Enantiomerically Pure Dibenzyl Esters of l

Jun 11, 2015(S)-Dibenzyl aspartate p-toluenesulfonate [(S)-1TsOH] and (S)-dibenzyl glutamate p-toluenesulfonate [(S)-2TsOH] were efficiently prepared from the respective l-amino acids and benzyl alcohol with very high yields by using cyclohexane as a water azeotroping solvent instead of benzene, carbon tetrachloride, toluene, or benzyl alcohol itself, as reported in literature methods.

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2 phenylethylamine hydrochloride 10 mg

Phenethylamine alkaloids originate (Table 16) from the amino acid l-tyrosine from small modifications in its molecule, 1 and they are classified as protoalkaloids because they do not have the nitrogen atom as part of the ring. 18 Commonly the phenethylamine derivatives are 3,4-di-or-3,4,5-trihydroxy-substituted compounds, obtained via dopamine.

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CA1268598A

ABSTRACT Peptide sweeteners, namely, ?-L-aspartyl-L-phenylalanine lower alkyl esters, especially the methyl estex are prepared from the corresponding ta.-lower alkyl ester by dissolving the ta.-lower alkyl ester in a mixed solvent and effecting intramolecular ester exchange, the hydrochloride of the desired ester is crystallized out; this method avoids production of the bitter tasting

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::S.V.Chem Intermediates (P) Ltd.,

10. D-Phenylglycine methyl ester hydrochloride 11. 4-Nitro-L-Phenylalanine methyl ester hydrochloride 12. Glycine ethyl ester hydrochloride 13. L-Methionine methyl ester hydrochloride 14. DL-Valine methytlester hydrochloride 15. DL-Tyrosine methylester hydrochloride 16. D-Leucine methyl ester hydrochloride 17. D-Isoleucine methyl ester

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Side Chain Protected Amino acids

We are offering side chain protected amino acids, amino acids, protected amino acids, essential amino acids, Fmoc-L-Aspartic Acid-Beta Allyl Ester, Fmoc-L-Lysine-Allyloxycarbonyloxy, Fmoc-L-Lys(Boc)-OH, N-Fmoc-S-Acetamidomethyl-L-Cystein and L-Glutamic Acid Dibenzyl Ester HCl.

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