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1H-Indazol-5-amine, 4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102170-46-7

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102170-46-7 Usage

Structure

A derivative of indazole with a nitro group at the 4-position of the indazole ring

Potential applications

Building block for the synthesis of various drug molecules in the pharmaceutical industry

Uses

Reagent in organic synthesis and medicinal chemistry research

Reactivity

Potentially reactive due to the presence of the nitro group, requiring careful handling in the laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 102170-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,7 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102170-46:
(8*1)+(7*0)+(6*2)+(5*1)+(4*7)+(3*0)+(2*4)+(1*6)=67
67 % 10 = 7
So 102170-46-7 is a valid CAS Registry Number.

102170-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-1H-indazol-5-amine

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:102170-46-7 SDS

102170-46-7Upstream product

102170-46-7Downstream Products

102170-46-7Relevant academic research and scientific papers

C-H Amination of Nitro Azaheterocyclic Compounds by Vicarious Nucleophilic Substitution

Zhou, Ru-Shuang,Cai, Chun

supporting information, p. 88 - 92 (2021/12/03)

Various nitro azaheterocyclic compounds were subjected to C H amination by vicarious nucleophilic substitution with 4H-1,2,4-triazol-4-amine (ATA). The aminated products were characterized by NMR, mass spectroscopy, and single-crystal X-ray diffraction an

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