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37662-06-9

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37662-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37662-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,6 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37662-06:
(7*3)+(6*7)+(5*6)+(4*6)+(3*2)+(2*0)+(1*6)=129
129 % 10 = 9
So 37662-06-9 is a valid CAS Registry Number.

37662-06-9Relevant articles and documents

2-Azanorbornane-Based Amino Alcohol Organocatalysts for Asymmetric Michael Reaction of β-Keto Esters with Nitroolefins

Togashi, Rei,Chennapuram, Madhu,Seki, Chigusa,Okuyama, Yuko,Kwon, Eunsang,Uwai, Koji,Tokiwa, Michio,Takeshita, Mitsuhiro,Nakano, Hiroto

, p. 3882 - 3889 (2019/06/21)

New optically active 2-azanorbornane-based amino alcohol organocatalysts were designed and synthesized, and these catalysts were successfully employed in the asymmetric Michael reaction of β-keto esters with nitroolefins to obtain the corresponding chiral

BIOLOGICALLY ACTIVE AMIDES

-

Page/Page column 38, (2010/06/11)

The present invention is directed to biologically active amides which are ligands at the NPY Y5 receptor. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from certain disorders which comprises administering to the subject an amount of a compound of the subject invention. Furthermore, this invention also provides uses of a compound of the invention for the manufacture of a medicament for treating a subject suffering from certain disorders.

The aza-Diels-Alder reaction protocol - A useful approach to chiral, sterically constrained α-amino acid derivatives

Bertilsson, Sophie K,Ekegren, Jenny K,Modin, Stefan A,Andersson, Pher G

, p. 6399 - 6406 (2007/10/03)

Different types of polycyclic α-amino acid derivatives are prepared from chiral imines by using well-established aza-Diels-Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15-21 are formed.

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