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Benzaldehyde, 2,4,5-trifluoro-, oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

581072-18-6

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581072-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 581072-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,1,0,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 581072-18:
(8*5)+(7*8)+(6*1)+(5*0)+(4*7)+(3*2)+(2*1)+(1*8)=146
146 % 10 = 6
So 581072-18-6 is a valid CAS Registry Number.

581072-18-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2,4,5-trifluorophenyl)methylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 2,4,5-Trifluorobenzaldehyde oxime

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:581072-18-6 SDS

581072-18-6Relevant academic research and scientific papers

Oxime Carbamate-Discovery of a series of novel FAAH inhibitors

Sit,Conway, Charles M.,Xie, Kai,Bertekap, Robert,Bourin, Clotilde,Burris, Kevin D.

supporting information; experimental part, p. 1272 - 1277 (2010/06/17)

A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.

Synthesis and biological activity of 3-substituted isoxazolecarboxamides

Gucma, Miroslaw,Golebiewski, W. Marek

scheme or table, p. 461 - 469 (2011/07/30)

A series of novel 3-substituted isoxazolecarboxamides have been prepared. A key step was 1,3-dipolar cycloaddition of nitrile oxides to α,β-unsaturated esters. Some of these compounds exhibited high fungicidal activities against Alternaria alternata, Botrytis cinerea, Rhizoctonia solani, Fusarium culmorum, and Phytophthora cactorum.

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