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2H-Indazole, 6-nitro-2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88369-83-9

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88369-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88369-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88369-83:
(7*8)+(6*8)+(5*3)+(4*6)+(3*9)+(2*8)+(1*3)=189
189 % 10 = 9
So 88369-83-9 is a valid CAS Registry Number.

88369-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-6-nitroindazole

1.2 Other means of identification

Product number -
Other names 2-Benzyl-6-nitro-2H-indazol

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:88369-83-9 SDS

88369-83-9Downstream Products

88369-83-9Relevant academic research and scientific papers

Selective synthesis of 1 -functionalized-alkyl-1H-indazoles

Hunt, Kevin W.,Moreno, David A.,Suiter, Nicole,Clark, Christopher T.,Kim, Ganghyeok

scheme or table, p. 5054 - 5057 (2009/12/28)

An efficient method for the selective "N1" alkylation of indazoles is described. Use of a-halo esters, lactones, ketones, amides, and bromoacetonitrile provides good to excellent yield of the desired N1 products.

Synthesis, structure elucidation and antibacterial activity of 6-ethyl-6,9-dihydro-9-oxopyrazolo[3,4-f]quinoline-8-carboxylic acid

Schwan,Freedman,Pollack

, p. 1351 - 1353 (2007/10/02)

The preparation, structure elucidation and antibacterial activity of 6-ethyl-6,9-dihydro-9-oxopyrazolo-[3,4-f]quinoline-8-carboxylic acid are reported.

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