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7188-94-5

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7188-94-5 Usage

Class

Aromatic heterocyclic compounds containing a five-membered ring with two nitrogen atoms and three carbon atoms

Structure

A derivative of pyrazole with a methyl group at the 3-position and two phenyl groups at the 1 and 4 positions

Usage

Building block in the synthesis of various pharmaceuticals and agrochemicals

Reactivity

Versatile

Functional group compatibility

High

Biological activities

Exhibits interesting biological activities

Importance in pharmaceutical industry

Valuable intermediate

Check Digit Verification of cas no

The CAS Registry Mumber 7188-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7188-94:
(6*7)+(5*1)+(4*8)+(3*8)+(2*9)+(1*4)=125
125 % 10 = 5
So 7188-94-5 is a valid CAS Registry Number.

7188-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1,4-diphenylpyrazole

1.2 Other means of identification

Product number -
Other names 3-methyl-1,4-diphenyl-1H-pyrazole

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:7188-94-5 SDS

7188-94-5Downstream Products

7188-94-5Relevant articles and documents

Pyrazole synthesis using a titanium-catalyzed multicomponent coupling reaction and synthesis of withasomnine

Majumder, Supriyo,Gipson, Kevin R.,Staples, Richard J.,Odom, Aaron L.

experimental part, p. 2013 - 2023 (2011/02/28)

The titanium-catalyzed 3-component coupling of an alkyne, isonitrile, and amine can be used to generate tautomers of 1,3-diimines. These diimines produced in situ undergo cyclization with hydrazine and hydrazine derivatives in a one-pot procedure to provi

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