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244017-81-0

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244017-81-0 Usage

Class

1H-indazoles (compounds containing an indazole moiety, which consists of a pyrazole ring fused to a benzene ring)

Subclass

Halogenated indazoles

Functional group

Chloroacetyl group (an acetyl group bonded to a chlorine atom)

Potential applications

Pharmaceuticals, agrochemicals, and materials science (specific properties and uses may vary depending on exact application and formulation)

Check Digit Verification of cas no

The CAS Registry Mumber 244017-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,0,1 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 244017-81:
(8*2)+(7*4)+(6*4)+(5*0)+(4*1)+(3*7)+(2*8)+(1*1)=110
110 % 10 = 0
So 244017-81-0 is a valid CAS Registry Number.

244017-81-0SDS

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-chloro-1-indazol-1-ylethanone

1.2 Other means of identification

Product number -
Other names 1-(CHLOROACETYL)-1H-INDAZOLE

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:244017-81-0 SDS

244017-81-0Downstream Products

244017-81-0Relevant articles and documents

Selective N1-Acylation of Indazoles with Acid Anhydrides Using an Electrochemical Approach

DIssanayake, D.M.M. Mevan,Vannucci, Aaron K.

supporting information, p. 457 - 460 (2019/01/23)

An electrochemical synthesis method for the selective N1-acylation of indazoles has been developed. This "anion pool" approach electrochemically reduces indazole molecules generating indazole anions and H2. Acid anhydrides are then introduced to the solution resulting in selective acylation of the N1-position of the indazoles. This procedure can also be applied to the acylation of benzimidazoles and indoles. The reaction can also be performed using a 9 V battery without loss of reaction efficiency.

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