CAS 201404-15-1

(2R)-3-benzylsulfanyl-2-[(2,2,2-trideuterioacetyl)amino]propanoic acid

Description:

(2R)-3-benzylsulfanyl-2-[(2,2,2-trideuterioacetyl)amino]propanoic acid is a chiral amino acid derivative characterized by the presence of a benzylsulfanyl group and a deuterated acetylamino moiety. The compound features a propanoic acid backbone, which contributes to its acidic properties. The presence of the benzylsulfanyl group introduces a sulfur atom, which can influence the compound's reactivity and potential interactions in biological systems. The deuterated acetyl group suggests that this compound may be used in studies involving isotopic labeling, which can aid in tracing metabolic pathways or understanding reaction mechanisms. The chirality of the molecule indicates that it may exhibit specific biological activities or interactions, as many biological systems are sensitive to the stereochemistry of amino acids. Overall, this compound's unique structural features make it of interest in both synthetic chemistry and potential pharmaceutical applications.

Formula: C₁₂H₁₂D₃NO₃S

InChI: InChI=1/C12H15NO3S/c1-9(14)13-11(12(15)16)8-17-7-10-5-3-2-4-6-10/h2-6,11H,7-8H2,1H3,(H,13,14)(H,15,16)/t11-/m0/s1/i1D3

SMILES: C(C(=N[C@@H](CSCc1ccccc1)C(=O)O)O)([2H])([2H])[2H]

N-(Acetyl-d3)-S-benzyl-L-Cysteine

CAS: 201404-15-1

Formula: C₁₂H₁₂D₃NO₃S

Molecular weight: 256.33

Ref: 4Z-C-77124

N-(Acetyl-d3)-S-benzyl-L-cysteine

Controlled Product

CAS: 201404-15-1

Applications A labelled metabolite of Toluene.
References Gargas, M., et al.: Toxicol. Appl. Pharmacol., 98, 87 (1989), Commandeur, J., et al.: Pharmacol. Rev., 47(2), 271 (1995), Campo, P., et al.: Neurotoxicol. Teratol., 21, 427 (1999), Lohse, C., et al.: J. Agr. Food Chem., 48, 5913 (2000),

Formula: C₁₂₂H₃H₁₂NO₃S

Color and Shape: White To Off-White

Molecular weight: 256.34

Ref: TR-A168427

L-Cysteine, N-(acetyl-d3)-S-(phenylmethyl)- (9CI)

CAS: 201404-15-1

Formula: C₁₂H₁₂D₃NO₃S

Color and Shape: Solid

Molecular weight: 256.3359

Ref: IN-DA002DDS