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Benzeneacetonitrile, a-formyl-3-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70806-40-5

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70806-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70806-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,0 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70806-40:
(7*7)+(6*0)+(5*8)+(4*0)+(3*6)+(2*4)+(1*0)=115
115 % 10 = 5
So 70806-40-5 is a valid CAS Registry Number.

70806-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-formyl-3-(trifluoromethyl)benzeneacetonitrile

1.2 Other means of identification

Product number -
Other names α-formyl-α-(3'-trifluoromethylphenyl)acetonitrile

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:70806-40-5 SDS

70806-40-5Downstream Products

70806-40-5Relevant academic research and scientific papers

Potential antimalarials. XXII Some 2,4-diamino-5-(3- and 4-trifluoromethylphenyl and 3,4-methylenedioxyphenyl)pyrimidines

Barlin, Gordon B.,Kotecka, Barbara,Rieckmann, Karl H.

, p. 647 - 650 (2007/10/03)

A series of 10 pyrimethamine analogues containing 3′- and 4′-trifluoromethyl and 3′,4′-methylenedioxy groups has been prepared and tested for in vitro antimalarial activity against the FC-27 and K-1 isolates of Plasmodium falciparum. Several of these compounds were almost as active as pyrimethamine against the drug-sensitive FC-27 isolate, and like pyrimethamine, they were much less active against the drug-resistant K-1 isolate. The 4′-trifluoromethyl compunds, however, showed much smaller differences.

Substituted 6-phenyl-1,2,4-triazolo[4,3-a]pyridines

-

, (2008/06/13)

This disclosure describes novel 6-(substituted-phenyl)-1,2,4-triazolo[4,3-a]pyridines useful as hypotensive agents.

Substituted 3-alkyl-6-phenyl-1,2,4-triazolo-[4,3-a]pyridines

-

, (2008/06/13)

This disclosure describes novel 3-alkyl-6-(substituted-phenyl)-1,2,4-triazolo[4,3-a]pyridines useful as anxiolytic agents.

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