150281-47-3 Usage
General Description
4-Pyrrolidin-3-yl-pyridine is a chemical compound that belongs to the class of organic compounds known as pyridinyl-pyrrolidines. These are compounds containing a pyridine ring which is substituted by a pyrrolidine ring at one or more positions. It has the molecular formula C9H12N2 and the molecular weight is 148.2 g/mol. While there is limited information available on the specific uses and properties of this compound, compounds in the pyridinyl-pyrrolidines class are typically part of complex molecular structures with a range of properties and uses in medicinal chemistry and other areas of science.
Check Digit Verification of cas no
The CAS Registry Mumber 150281-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,2,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150281-47:
(8*1)+(7*5)+(6*0)+(5*2)+(4*8)+(3*1)+(2*4)+(1*7)=103
103 % 10 = 3
So 150281-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2/c1-4-10-5-2-8(1)9-3-6-11-7-9/h1-2,4-5,9,11H,3,6-7H2
150281-47-3Relevant articles and documents
Synthesis of 3-substituted pyrrolidines
Kurkin,Sumtsova,Yurovskaya
, p. 34 - 40 (2007/10/03)
A method was developed for the synthesis of derivatives of 3-substituted pyrrolidines from activated alkenes by 1,3-dipolar cycloaddition of unstable 2-benzylazomethylide, generated in situ from N-benzyl-N-(methoxymethyl)-N- (trimethylsilyl)amine. A method was developed for the reduction of 4-(3-pyrrolidyl)pyridine, prepared by the above-mentioned method, to the corresponding derivatives of (3-pyrrolidyl)piperidine with high yields under mild conditions.
7-substituted quinolones and naphthyridones as antibacterial agents
-
, (2008/06/13)
7-Substituted quinolones and naphthyridones are described as antibacterial agents as well as a process for their manufacture, compositions therefor, wherein the 7-substituent is a pyrrolidine ring substituted at the 3-position by a substituted aromatic hydrocarbon or a heteroaromatic group.