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5964-48-7

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5964-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5964-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5964-48:
(6*5)+(5*9)+(4*6)+(3*4)+(2*4)+(1*8)=127
127 % 10 = 7
So 5964-48-7 is a valid CAS Registry Number.

5964-48-7Downstream Products

5964-48-7Relevant articles and documents

Discovery of the first M5-selective and CNS penetrant negative allosteric modulator (NAM) of a muscarinic acetylcholine receptor: (S)-9b-(4-chlorophenyl)-1-(3,4-difluorobenzoyl)-2,3-dihydro-1 H -imidazo[2,1- a ]isoindol-5(9b H)-one (ML375)

Gentry, Patrick R.,Kokubo, Masaya,Bridges, Thomas M.,Kett, Nathan R.,Harp, Joel M.,Cho, Hyekyung P.,Smith, Emery,Chase, Peter,Hodder, Peter S.,Niswender, Colleen M.,Daniels, J. Scott,Conn, P. Jeffrey,Wood, Michael R.,Lindsley, Craig W.

, p. 9351 - 9355 (2013)

A functional high throughput screen and subsequent multidimensional, iterative parallel synthesis effort identified the first muscarinic acetylcholine receptor (mAChR) negative allosteric modulator (NAM) selective for the M5 subtype. ML375 is a

POLYCYCLIC AGENTS FOR THE TREATMENT OF RESPIRATORY SYNCYTIAL VIRUS INFECTIONS

-

Page/Page column 41, (2010/02/12)

Compounds of formula (I), and their use as in the treatment of infections involving viruses of the Pneumovirinae sub-family (RSV) are disclosed. In the formula ring (A) may be phenyl, pyridyl etc., (B-C) may be CH2-CH2etc., (R1) may be phenyl and substituted forms thereof, (R2) may be assorted substituents.

5H-imidazo[2,1-a]isoindol-5-one compounds

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, (2008/06/13)

A new class of chemical compounds whose members exert an appetite suppressant and mood elevating effect in man has been invented. This class is defined as being composed of those compounds having the 1-substituted-2,5-benzodiazocine structure, fully saturated in the nonbenzenoid portion, and whose nitrogens are tervalent. Members of this class are prepared by condensing an orthobenzoylbenzoic acid or ester thereof with an ethylenediamine and reducing with a metallic alkaline hydride the product thus obtained.

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