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1H-Indazol-6-amine, 1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51336-56-2

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51336-56-2 Usage

Derivative of

Indazole

Contains

An amine group and a phenylmethyl group

Commonly used in

Synthesis of various pharmaceuticals and research chemicals

Has

Potential pharmacological properties

Of interest in

Medicinal chemistry for its potential therapeutic activities

Valuable for

Creating diverse molecular structures and exploring new chemical reactions and processes

Check Digit Verification of cas no

The CAS Registry Mumber 51336-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51336-56:
(7*5)+(6*1)+(5*3)+(4*3)+(3*6)+(2*5)+(1*6)=102
102 % 10 = 2
So 51336-56-2 is a valid CAS Registry Number.

51336-56-2SDS

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 1-benzyl-1H-indazol-6-ylamine

1.2 Other means of identification

Product number -
Other names 1-Benzyl-1H-indazol-6-ylamin

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:51336-56-2 SDS

51336-56-2Relevant academic research and scientific papers

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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