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tert-butyl 4-[(4-bromo-5-methyl-2-nitrophenyl)amine]piperidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

932374-60-2

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932374-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 932374-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,3,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 932374-60:
(8*9)+(7*3)+(6*2)+(5*3)+(4*7)+(3*4)+(2*6)+(1*0)=172
172 % 10 = 2
So 932374-60-2 is a valid CAS Registry Number.

932374-60-2Relevant academic research and scientific papers

Preparation of a first 18F-labeled agonist for M1 muscarinic acetylcholine receptors

Drewes, Birte,Kolks, Niklas,Neumaier, Bernd,Neumaier, Felix,Rüngeler, Till,Zlatopolskiy, Boris D.

, (2020)

M1 muscarinic acetylcholine receptors (mAChRs) are abundant in postsynaptic nerve terminals of all forebrain regions and have been implicated in the cognitive decline associated with Alzheimer’s disease and other CNS pathologies. Consequently,

SUBSTITUTED BENZIMIDAZOLONE COMPOUNDS

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Paragraph 53-54, (2020/11/23)

Disclosed are compounds of Formula (I) N-oxides, or salts thereof, wherein G, A, R1, and n are defined herein. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating inflammatory and autoimmune diseases.

COMPOUNDS WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE

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Page/Page column 58, (2010/11/26)

Compounds of formula (I) and salts and solvates are provided: In a first aspect therefore, the invention provides a compound of formula (I) or a salt or solvate thereof: wherein R5 is selected from halogen, C1-6alkyl, C1-6alkyl substituted with one or more fluorine atoms, C1-6 alkoxy, C1-6 alkoxy substituted with one or more fluorine atoms, and cyano; R6 is selected from halogen, C1-6alkyl, C1-6alkyl substituted with one or more fluorine atoms, C3-6cycloalkyl, C3-6cycloalkyl substituted with one or more fluorine atoms, C1-6 alkoxy, C1-6 alkoxy substituted with one or more fluorine atoms, and cyano; and Q is hydrogen or C 1-6 alkyl. The compounds are M1 agonists and are useful for therapy, for example in the treatment of psychotic disorders and cognitive impairment.

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