2517-07-9 Usage
Description
Methylenecyclopropylglycine, a homolog of Hypoglycine A, is an unusual amino acid derived from Litchi chinensis seeds. It exhibits antimutagenic properties, making it a potential candidate for various applications in the field of health and medicine.
Uses
Used in Antimutagenic Applications:
Methylenecyclopropylglycine is used as an antimutagenic agent for its ability to counteract spontaneous mutation in Salmonella typhimurium TA. This property suggests its potential use in preventing or reducing the risk of genetic mutations that may lead to various health issues.
Used in Pharmaceutical Industry:
Methylenecyclopropylglycine is used as a key component in the development of drugs targeting genetic mutations and related disorders. Its antimutagenic activity makes it a valuable asset in the creation of pharmaceuticals aimed at improving human health and well-being.
Used in Research and Development:
Methylenecyclopropylglycine is utilized as a research tool for studying the mechanisms of genetic mutations and the development of potential countermeasures. Its unique properties allow scientists to gain a deeper understanding of mutation processes and the ways in which they can be mitigated or prevented.
Check Digit Verification of cas no
The CAS Registry Mumber 2517-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2517-07:
(6*2)+(5*5)+(4*1)+(3*7)+(2*0)+(1*7)=69
69 % 10 = 9
So 2517-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO2/c1-3-2-4(3)5(7)6(8)9/h4-5H,1-2,7H2,(H,8,9)/t4-,5-/m0/s1
2517-07-9Relevant articles and documents
Synthesis of (±)-(2-methylenecyclopropyl)glycine and (±)-4-[amino(carboxymethyl)]spiro[2.2]pentane-1-carboxylie acid
Averina, Elena B.,Yashin, Nikolai V.,Grishin, Yurii K.,Kuznetsova, Tamara S.,Zefirov, Nikolai S.
, p. 880 - 884 (2007/10/03)
A facile method for the preparation of racemic cyclopropylglycines is described, involving oxidation of cyclopropylcarbinols followed by a Bucherer-Berg reaction with sequential hydrolysis of the hydantoins obtained. Georg Thieme Verlag Stuttgart.
