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6-chloro-2-(3,5-dimethyl-1H-pyrazol-1-yl)-4-methylquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108936-72-7

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108936-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108936-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,3 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108936-72:
(8*1)+(7*0)+(6*8)+(5*9)+(4*3)+(3*6)+(2*7)+(1*2)=147
147 % 10 = 7
So 108936-72-7 is a valid CAS Registry Number.

108936-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,6-chloro-2-(3,5-dimethyl-1H-pyrazol-1-yl)-4-methyl

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:108936-72-7 SDS

108936-72-7Downstream Products

108936-72-7Relevant academic research and scientific papers

Synthesis of Some 2-(3',5'-Dimethylpyrazol-1'-yl)-4-methyl-6-substituted-quinolines and Their 4'-Substituted Analogues

Singh, S. P.,Vaid, R. K.,Prakash, I.,Prakash, O.

, p. 945 - 950 (2007/10/02)

The reaction of 2-hydrazinoquinolines (2) with pentane-2,4-dione yields pyrazoles (1) instead of the reported diazepines (3).The structural assignment is based on a rigorous spectral analysis of the product and on unambiguous synthesis.Several pyrazolylquinolines (1, 6 and 7) bearing a variety of substituents were synthesized and evaluated for their antiinflammatory and antimalarial activities.

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