100710-37-0 Usage
General Description
2-Naphthalen-2-yl-pyrrolidine is a chemical compound that consists of a pyrrolidine ring with a 2-naphthalenyl group attached to it. It is a white to off-white crystalline solid with a molecular formula of C16H17N. 2-NAPHTHALEN-2-YL-PYRROLIDINE is primarily used as a building block in the synthesis of various pharmaceuticals and other organic compounds. It has been shown to exhibit potential pharmacological activities, including anticonvulsant and antinociceptive properties. Additionally, 2-naphthalen-2-yl-pyrrolidine may also have potential applications in the field of organic electronics and materials science due to its unique structural properties.
Check Digit Verification of cas no
The CAS Registry Mumber 100710-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100710-37:
(8*1)+(7*0)+(6*0)+(5*7)+(4*1)+(3*0)+(2*3)+(1*7)=60
60 % 10 = 0
So 100710-37-0 is a valid CAS Registry Number.
100710-37-0Relevant articles and documents
CHIRAL CATALYST AND METHOD FOR ASYMMETRIC REDUCTION OF AN IMINE
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Paragraph 00185; 00186; 00187, (2019/04/16)
The present disclosure discusses (i) a compound having a chemical formula according to Formula (I), or its enantiomer; and (ii) a compound that is reactive with a hydride to produce a compound having a chemical formula according to Formula (I), or its enantiomer. Formula (I) is: Formula (I) where R1 and R2 are H, optionally substituted C1-C3 alkyl, or linked together to form an optionally substituted C3 or C4 alkyl group; R3 and R3' are H; R4 and R4' are the same, and are optionally substituted C1-C6 alkyl; and R5 and R5' are the same, and are optionally substituted aryl or heteroaryl. In some examples, R4 and R5 are linked, and R4' and R5' are linked, where both linking groups are the same. The present disclosure also discusses methods of asymmetric reduction of an imine, and methods of forming the catalysts and pre-catalysts.
