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1178903-41-7

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1178903-41-7 Usage

Type of compound

Nitroindazole derivative

Substituent group

4-Methoxybenzyl group attached to the nitrogen atom

Potential pharmacological activities

Antimicrobial and antitumor properties

Application

Building block in organic synthesis and medicinal chemistry

Importance

Valuable for further research and potential drug development

Check Digit Verification of cas no

The CAS Registry Mumber 1178903-41-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,8,9,0 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1178903-41:
(9*1)+(8*1)+(7*7)+(6*8)+(5*9)+(4*0)+(3*3)+(2*4)+(1*1)=177
177 % 10 = 7
So 1178903-41-7 is a valid CAS Registry Number.

1178903-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-2-(4-methoxybenzyl)-2H-indazole

1.2 Other means of identification

Product number -
Other names 2-(4-methoxybenzyl)-5-nitro-2H-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:1178903-41-7 SDS

1178903-41-7Downstream Products

1178903-41-7Relevant articles and documents

Indazoles: Regioselective protection and subsequent amine coupling reactions

Slade, David J.,Pelz, Nicholas F.,Bodnar, Wanda,Lampe, John W.,Watson, Paul S.

supporting information; experimental part, p. 6331 - 6334 (2009/12/26)

(Chemical Equation Presented) Indazoles are unselectively protected under strongly basic conditions to give a mixture at N-1 and N-2. Under mildly acidic conditions, regioselective protection at N-2 takes place. Thermodynamic conditions lead to regioselective protection at N-1. This trend applies to various substituted indazoles. Protected 5-bromoindazoles participate in Buchwald reactions with a range of amines to generate novel derivatives.

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