89422-41-3 Usage
Uses
Used in Chemical and Biochemical Research:
(N-TRIFLUOROACETYL-L-CYSTEINYL)GLYCINE METHYL ESTER, (1-1') DISULPHIDE is used as a research reagent for investigating protein structure and function. The presence of the disulfide bond enables the formation of intraand intermolecular bridges, which are crucial for protein folding and stability.
Used in the Study of Oxidative Stress and Redox Signaling:
(N-TRIFLUOROACETYL-L-CYSTEINYL)GLYCINE METHYL ESTER, (1-1') DISULPHIDE serves as a valuable tool in understanding the mechanisms of oxidative stress and redox signaling due to its unique chemical properties, including the trifluoroacetyl group.
Used in Pharmaceutical Development:
(N-TRIFLUOROACETYL-L-CYSTEINYL)GLYCINE METHYL ESTER, (1-1') DISULPHIDE may be employed as a starting material or intermediate in the development of pharmaceuticals targeting protein-related diseases and conditions influenced by oxidative stress and redox signaling.
Used in Material Science:
The unique properties of the disulfide bond and the trifluoroacetyl group in (N-TRIFLUOROACETYL-L-CYSTEINYL)GLYCINE METHYL ESTER, (1-1') DISULPHIDE may also find applications in the development of novel materials with specific chemical and physical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 89422-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89422-41:
(7*8)+(6*9)+(5*4)+(4*2)+(3*2)+(2*4)+(1*1)=153
153 % 10 = 3
So 89422-41-3 is a valid CAS Registry Number.
89422-41-3Relevant academic research and scientific papers
Total synthesis of slow reacting substances (SRS). "Leukotriene C-2" (11-trans-leukotriene C) (3) and leukotriene D (4)
Corey,Clark, David A.,Marfat, Anthony,Goto, Giichi
, p. 3143 - 3146 (2007/10/02)
Syntheses are described for the "slow reacting substances" 11-trans-leukotriene C (3) (previously known as leukotriene C-2) and leukotriene D (4), the cys-gly analog of leukotriene C (2). The synthesized leukotrienes 3 and 4 were instrumental in the assignment of structure to these members of the family of naturally occuring slow reacting substances which includes also 2.
