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151025-70-6

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151025-70-6 Usage

Chemical Structure

Quinoline derivative with two trifluoromethyl groups (2, 8 positions) and a cyano group (4 position)

Common Uses

Building block in organic synthesis, medicinal chemistry

Biological Activities

Studied for potential as a pharmaceutical intermediate, precursor in synthesis of bioactive compounds

Properties

High lipophilicity, chemical stability due to trifluoromethyl groups

Check Digit Verification of cas no

The CAS Registry Mumber 151025-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151025-70:
(8*1)+(7*5)+(6*1)+(5*0)+(4*2)+(3*5)+(2*7)+(1*0)=86
86 % 10 = 6
So 151025-70-6 is a valid CAS Registry Number.

151025-70-6SDS

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 2,8-bis(trifluoromethyl)quinoline-4-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:151025-70-6 SDS

151025-70-6Downstream Products

151025-70-6Relevant articles and documents

{SEQ CHAPTER h r l} Synthesis of novel trifluoromethylquinoline and bis(trifluoromethyl)quinoline derivatives

Kgokong, Joseph L.,Breytenbach, Jaco C.

, p. 100 - 103 (2007/10/03)

Six new 2- and 8-trifluoromethyl- and 2,8-bis(trifluoromethyl)quinolin-4-yl ketones were synthesised and evaluated for in vitro antimalarial activity. The ketones were prepared by condensation of the corresponding quinoline-4-carboxylic acids with pyrimidin-5-yllithium or [(1-ethyl-5-nitro-1H-imidazol-4-yl)methyl]lithium. The new compounds showed slight in vitro antimalarial activity against the chloroquine-sensitive strain of Plasmodium falciparum.

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