312746-71-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
D-S-Isoamylcysteine is utilized as a precursor in the synthesis of peptides and proteins, which are fundamental components in the development of various pharmaceuticals and agrochemicals. Its role in these syntheses is crucial for creating bioactive molecules with specific therapeutic or pesticidal properties.
Used in Medicinal Chemistry Research:
Due to its potential antioxidant and anti-inflammatory properties, D-S-Isoamylcysteine is employed in medicinal chemistry research. These properties make it a candidate for the development of new drugs that could treat a range of conditions associated with oxidative stress and inflammation.
Used in Industrial and Environmental Applications:
D-S-Isoamylcysteine's chelating properties allow it to form stable complexes with metal ions. This makes it useful in industrial processes where metal ion management is necessary, as well as in environmental applications for the remediation of metal contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 312746-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,7,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 312746-71:
(8*3)+(7*1)+(6*2)+(5*7)+(4*4)+(3*6)+(2*7)+(1*1)=127
127 % 10 = 7
So 312746-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2S/c1-6(2)3-4-12-5-7(9)8(10)11/h6-7H,3-5,9H2,1-2H3,(H,10,11)/t7-/m1/s1
312746-71-7Relevant academic research and scientific papers
Asymmetric synthesis of S-alkyl-substituted (R)-cysteines via a chiral NiII complex of the Schiff's base of dehydroalanine with (S)-2-N-(N-benzylprolyl)aminobenzophenone
Saghiyan,Geolchanyan,Djamgaryan,Vardapetyan,Tararov,Kuz'mina,Ikonnikov,Belokon',North
, p. 1460 - 1463 (2007/10/03)
An efficient procedure was developed for the asymmetric synthesis of S-alkyl derivatives of (R)-cysteine by nucleophilic addition of alkanethiols (BunSH, ButSH, or tert-C5H11SH) to the C=C bond of the dehydroalanine fragment in the Ni11 complex of the Schiff's base of Δ-Ala with (S)-2-N-(N-benzylprolyl)aminobenzophenone [(S)-BPB-Δ-Ala]Ni11. Under conditions of thermodynamic control of the reaction, the diastereomeric excess of the complexes with the (S,R)-configuration was 88 - 96%. After decomposition of the complexes, (R)-S-butylcysteine, (R)-S-tert-butylcysteine, and (R)-S-tert-pentylcysteine were isolated with an enantiomeric purity of >97%.
