1432-27-5 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-2-[(ammonioacetyl)amino]-3-(1H-indol-3-yl)propanoate is used as a pharmaceutical compound for its potential interactions with biological systems. Due to its structural similarity to tryptophan, it may have applications in the development of drugs targeting specific enzymes or receptors, contributing to treatments for various diseases and conditions.
Used in Biochemical Research:
In the field of biochemistry, (2R)-2-[(ammonioacetyl)amino]-3-(1H-indol-3-yl)propanoate serves as a valuable research tool. Its unique structure allows scientists to study its interactions with enzymes and receptors, potentially leading to a better understanding of biological processes and the discovery of new therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 1432-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1432-27:
(6*1)+(5*4)+(4*3)+(3*2)+(2*2)+(1*7)=55
55 % 10 = 5
So 1432-27-5 is a valid CAS Registry Number.
1432-27-5Relevant academic research and scientific papers
PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE SYNTHESIS. USE OF A NEW DERIVATIVE, Nin-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHAN
Kiso, Yoshiaki,Inai, Masatoshi,Kitagawa, Kouki,Akita, Tadashi
, p. 739 - 742 (2007/10/02)
The 2,2,2-trichloroethoxycarbonyl (Troc) group attached at the Nin function of tryptophan by acylation with Troc-Cl in the presence of a catalytic amount of tetra-n-butylammonium hydrogensulfate can be quantitatively removed either by cadmium dust in acetic acid or under basic conditions, e. g., hydrazine hydrate and NaOH, but is resistant to strong acidic conditions.
