1256643-67-0 Usage
Description
(1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is a chemical compound that is a derivative of imidazole, a five-membered heterocyclic compound containing two nitrogen atoms. It is commonly found in salts such as HCl and is often used in pharmaceutical research and drug development.
Used in Pharmaceutical Research and Drug Development:
(1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is used as a pharmaceutical compound for its potential therapeutic benefits in antifungal and antihypertensive medications. The addition of HCl to this compound likely alters its solubility, stability, and other properties, making it more suitable for certain applications in the pharmaceutical industry.
Used in Antifungal Medications:
(1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is used as an antifungal agent for its potential to treat fungal infections.
Used in Antihypertensive Medications:
(1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is used as an antihypertensive agent for its potential to treat high blood pressure.
Used in Central Nervous System Disorders:
(1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is used as a potential treatment for anxiety and other central nervous system disorders due to its potential therapeutic benefits.
Overall, (1-benzyl-1H-imidazol-5-yl)acetonitrile(SALTDATA: HCl) is a promising compound with potential therapeutic benefits and is of interest for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1256643-67-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,6,4 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1256643-67:
(9*1)+(8*2)+(7*5)+(6*6)+(5*6)+(4*4)+(3*3)+(2*6)+(1*7)=170
170 % 10 = 0
So 1256643-67-0 is a valid CAS Registry Number.
1256643-67-0Relevant articles and documents
A versatile, enantioselective, stereocontrolled synthesis of (1S,2R)-imidazoleglycerol
Paz, Manuel M.,Correa, Juan F.,Cabeza, M. Isabel,Sardina, F. Javier
, p. 9259 - 9262 (1996)
An efficient (21% overall yield), enantio- and diastereoselective, 11-step synthesis of (1S,2R)-imidazoleglycerol has been developed. The key steps are the stereoselective hydroxylation of an acyloxazolidinone enolate, the alkylation of a thioester with (MOMOCH2)2CuLi and the stereodivergent reduction of the resulting ketone. The scope of the reaction of the enolate derived from 10 with heteroatom electrophiles has been studied.
