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141278-23-1

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141278-23-1 Usage

Type of compound

heterocyclic organic compound (indazole derivative)

Contains

chlorine atom, nitro group, oxirane (epoxy) group

Biological activities

anti-inflammatory, analgesic, antimicrobial properties

Potential applications

pharmacology and medicinal chemistry for new drug development

Check Digit Verification of cas no

The CAS Registry Mumber 141278-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,7 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141278-23:
(8*1)+(7*4)+(6*1)+(5*2)+(4*7)+(3*8)+(2*2)+(1*3)=111
111 % 10 = 1
So 141278-23-1 is a valid CAS Registry Number.

141278-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chlor-1-(2,3-epoxypropyl)-5-nitroindazol

1.2 Other means of identification

Product number -
Other names 3-Chloro-5-nitro-1-oxiranylmethyl-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:141278-23-1 SDS

141278-23-1Downstream Products

141278-23-1Relevant articles and documents

Azoles. Part 32: Nitroindazole derivatives and their electron affinity

Usarewicz,Wrzeciono,Lukaszewski,Gatniejewska,Peisert

, p. 15 - 18 (2007/10/02)

A modified procedure for the synthesis of the dinitroindazoles 5-8 is described. Treatment of the chloronitro- and dinitroindazoles 1-8 with epichlorohydrin afforded the chlorohydroxypropyl- and epoxypropylindazole derivatives 2a-8a, 1b-5b, 7b and 7c. The structure of the compounds is confirmed by the aid of their IR, 1H and 13C NMR spectra. The electron affinity of the nitroindazole derivatives 1-16 is discussed on the basis of their halfwave potentials and in the combination with their eventual radiosensitizing properties.

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