536742-69-5 Usage
Uses
Used in Pharmaceutical Research and Development:
1-(4-Fluorophenyl)pyrrolidin-3-one is used as a precursor or intermediate in the synthesis of various pharmaceuticals and research chemicals. Its unique structure and potential pharmacological activity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Scientific Communities:
The properties and uses of 1-(4-Fluorophenyl)pyrrolidin-3-one are of interest to the pharmaceutical and scientific communities. Researchers and scientists explore its potential applications and interactions within biological systems to further understand its role in drug discovery and medicinal chemistry.
It is important to handle and use 1-(4-Fluorophenyl)pyrrolidin-3-one with caution due to its potential reactivity and toxicity. Proper safety measures should be taken to minimize risks associated with its use in research and development settings.
Check Digit Verification of cas no
The CAS Registry Mumber 536742-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,4 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 536742-69:
(8*5)+(7*3)+(6*6)+(5*7)+(4*4)+(3*2)+(2*6)+(1*9)=175
175 % 10 = 5
So 536742-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10FNO/c11-8-1-3-9(4-2-8)12-6-5-10(13)7-12/h1-4H,5-7H2
536742-69-5Relevant articles and documents
Non-classical antifolates, 5-(N-phenylpyrrolidin-3-yl)-2,4,6-triaminopyrimidines and 2,4-Diamino-6(5H)-oxopyrimidines, synthesis and antitumor studies
Huang, Yen-Lin,Lin, Chyun-Feng,Lee, Yi-Jen,Li, Wei-Wei,Chao, Ting-Chou,Bacherikov, Valeriy A.,Chen, Kuo-Tung,Chen, Chin-Ming,Su, Tsann-Long
, p. 145 - 157 (2007/10/03)
A series of non-classical antifolates, namely 5-(N-phenylpyrrolidin-3-yl)-2,4,6-triaminopyrimidines (25a-i) and 2,4-diamino-(N-phenylpyrrolidin-3-yl)-6(5H)-oxopyrimidines (26a,b,c,f,h,i) was synthesized and evaluated for their in vitro cytotoxicity. React
6,7-dihydropyrrol[3,4-c]pyrido[2,3-d]pyrimidine derivatives
-
, (2008/06/13)
The present invention concerns compounds of the formula: STR1 wherein R is a lower alkyl group, an aryl group or an alkylaryl group and X and Y are the same or different, and each is OH, NH2, or SH. The aryl group or the aryl moiety of the alkylaryl group may be unsubstituted, monosubstituted, disubstituted or trisubstituted. If substituted, each substituent may independently be an alkyl group, an alkyloxy group or a halogen. The present invention also provides methods for synthesizing the compounds described above.
