57866-70-3

Basic information

• Product Name: S-benzyl(2-2H1)DL-cysteine
• Synonyms: S-Benzyl(2-2H1)DL-cysteine; S-benzyl(2-~2~H)cysteine; S-benzylcysteine
• CAS NO: 57866-70-3
• Molecular Formula: C₁₀H₁₃NO₂S
• Molecular Weight: 211.2807
• EINECS: 260-999-6
• Mol File: 57866-70-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 379.2°C at 760 mmHg
• Flash Point: 183.2°C
• Density: 1.258g/cm³
• Vapor Pressure: 1.99E-06mmHg at 25°C
• Refractive Index: 1.608
• CAS DataBase Reference: S-benzyl(2-2H1)DL-cysteine(CAS DataBase Reference)
• NIST Chemistry Reference: S-benzyl(2-2H1)DL-cysteine(57866-70-3)
• EPA Substance Registry System: S-benzyl(2-2H1)DL-cysteine(57866-70-3)

Safety Data

• Hazardous Substances Data: 57866-70-3(Hazardous Substances Data)

Upstream product

• 19538-71-7 N-acetyl-S-benzyl-D,L-cysteine 
• 57866-79-2 N-acetyl-S-benzyl-DL-(α-(2)H)cysteine 

Downstream Products

• 57866-71-4 S-benzyl<2-(2)H1>-L-cysteine 

Relevant articles and documents

Racemization Mechanism of Cysteine Dipeptide Active Ester Derivatives

The racemization rate constants of Z-Gly-L-Cys(Bzl)-OH and Z-L-Cys(Bzl)-OH active esters were practically identical, even though glycyl dipeptide active esters usually racemize 50-100 times faster than the amino acid active esters.This observation led to the conclusion that Z-Gly-L-Cys(Bzl)-ONp and other active estrs do not racemize through the 5(4H)-oxazolone but through an enolization mechanism.The deuterium isotope effect was used to demonstrate that the removal of the α-hydrogen in the racemization is indeed the rate-determining step.Ac-Cys(Bzl)-OH was convertedwith DCC to the 5(4H)-oxazolone and deuterated with AcO2H: during this procedure Ac2O and Ac-(α-2H)-DL-Cys(Bzl)-OH were formed, the latter was resolved with acylase I in the presence of Co(2+) ions.H(α-2H)-L-Cys(Bzl)-OH (II) was converted through Z-(α-2)-L-Cys(Bzl)-OH (V), Z-(α-2H)-L-Cys(Bzl)-ONp (VI), and HBr*H-(α-2H)-L-Cys(Bzl)-ONp (VII) to Z-Gly-(α-2H)-L-Cys(Bzl)-ONp (VIII).The racemization rate constant kr2H for deuterated VIII in THF with Et3N was 335 * 10-6 M-1 s-1, while the kτ(H) for the undeuterated VIII was 704 * 10-6 M-1 s-1, indicating an isotope effect of 2.1.The 5(4H)- and 5(42H)-oxazolones, XII and XIII, were prepared from Z-Gly-L-Cys(Bzl)-OH and Z-Gly-(α-2H)-L-Cys(Bzl)-OH with DCC under controlled conditions in 73percent optical purity.Racemization of XII and XIII with Et3N in THF is instantaneous while the coupling rate with H-Val-OMe is kc = 8.5*10-2 M-1 s-1; that is, kr >> kc.The racemization rate of 5(4H)-oxazolone XII during coupling with H-Val-OMe is 0.34 M-1 s-1, while the autoracemization rate of XII is 0.08 M-1 s1-.These results support the conclusions that Z-Gly-Cys(Bzl)-ONp racemizes mainly through an enolization mechanism and that the cysteine side chain is responsible for this abnormal behavior.It is expected in practical peptide synthesis that coupling cysteine dipeptide active esters will yield an optically purer product than the coupling of cysteine active ester derivatives.