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[1-(3-Chloro-phenyl)-meth-(E)-ylidene]-ethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82605-83-2

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82605-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82605-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82605-83:
(7*8)+(6*2)+(5*6)+(4*0)+(3*5)+(2*8)+(1*3)=132
132 % 10 = 2
So 82605-83-2 is a valid CAS Registry Number.

82605-83-2Relevant academic research and scientific papers

ACYCLIC HYDRAZIDES AS CANNABINOID RECEPTOR MODULATORS

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Page/Page column 40, (2010/11/08)

The acyclic hydrazides of the invention are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present inventio

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

Reaction of Thiiranes with Azomethine Compounds

Sokolov, V. V.,Ogloblin, K. A.,Potekhin, A. A.

, p. 470 - 475 (2007/10/02)

Thiiranes add to imines and oximes to give thiazolidines.The addition of asymmetrical thiiranes is regioselective.The reaction of derivatives of asymmetrical carbonyl compounds with methylthiirane leads to mixtures of cis and trans stereoisomers of thiazo

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