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1H-Pyrazole-4-carboxaldehyde, 5-chloro-3-methyl-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68827-40-7

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68827-40-7 Usage

Molecular Weight

270.7

Structure

A pyrazole ring with a carboxaldehyde group (-CHO) attached to the 4-position, a 5-chloro group at the 5-position, a 3-methyl group at the 3-position, and a phenylmethyl group (-CH2Ph) attached to the 1-position.

Class

Pyrazole derivatives

Potential Applications

Pharmaceutical and agrochemical industries as a building block for the synthesis of bioactive compounds, research and development for the creation of new chemical entities with diverse biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 68827-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,2 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68827-40:
(7*6)+(6*8)+(5*8)+(4*2)+(3*7)+(2*4)+(1*0)=167
167 % 10 = 7
So 68827-40-7 is a valid CAS Registry Number.

68827-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-chloro-3-methylpyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-benzyl-5-chloro-3-methyl-1H-pyrazole-4-carbaldehyde

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:68827-40-7 SDS

68827-40-7Upstream product

68827-40-7Relevant academic research and scientific papers

Synthesis of poly-functionalized pyrazoles under Vilsmeier-Haack reaction conditions

Popov, Aleksandr V.,Kobelevskaya, Valentina A.,Larina, Ludmila I.,Rozentsveig, Igor B.

, p. 1 - 14 (2019)

Synthesis of 1,3-disubstituted 5-chloro-1H-pyrazole-4-carbaldehydes was achieved by formylation of the corresponding 5-chloro-1H-pyrazoles under Vilsmeier-Haack conditions.

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