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1-ethyl-1H-pyrazole-3-carbonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1006471-16-4

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1006471-16-4 Usage

Type of compound

Carbonyl chloride derivative

Parent compound

1-Ethyl-1H-pyrazole-3-carboxylic acid

Usage

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Physical appearance

Colorless to pale yellow liquid

Odor

Pungent

Hazards

Corrosive to skin, eyes, and respiratory system

Handling precautions

Handle with caution, store in a cool, dry place away from heat and open flame

Common applications

Primarily used in research and development, not commonly found in consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 1006471-16-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,4,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1006471-16:
(9*1)+(8*0)+(7*0)+(6*6)+(5*4)+(4*7)+(3*1)+(2*1)+(1*6)=104
104 % 10 = 4
So 1006471-16-4 is a valid CAS Registry Number.

1006471-16-4SDS

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 1-Ethyl-1H-pyrazole-3-carbonyl chloride

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:1006471-16-4 SDS

1006471-16-4Downstream Products

1006471-16-4Relevant academic research and scientific papers

An efficient synthesis of isomeric 1-(1-Alkyl-1H-pyrazolyl) ethanones

Taydakov, Ilya,Krasnoselskiy, Sergey

, p. 1422 - 1424 (2013/02/23)

A simple and versatile general method for the preparation of N-substituted 3-, 4-, or 5-acetylpyrazoles from corresponding acids via hydrolysis and decarboxylation of substituted diethyl [(1-alkyl-1H-pyrazolyl)carbonyl]malonates was developed. Title compounds were prepared in three steps without isolation of intermediates in 48-82% overall yield.

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