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5686-93-1

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5686-93-1 Usage

General Description

3-Indazolinone is a chemical compound with the molecular formula C9H7N3O. It is a heterocyclic organic compound, and its structure consists of a benzene ring fused to an oxazole ring. 3-Indazolinone is widely used in the pharmaceutical industry as a building block for the synthesis of various biologically active compounds. It has been studied for its potential in the development of new drugs, particularly in the field of oncology and central nervous system disorders. Additionally, 3-Indazolinone has been researched for its antimicrobial and antiviral properties, making it a promising candidate for the development of new antibiotics and antiviral drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 5686-93-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5686-93:
(6*5)+(5*6)+(4*8)+(3*6)+(2*9)+(1*3)=131
131 % 10 = 1
So 5686-93-1 is a valid CAS Registry Number.

5686-93-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name indazol-3-one

1.2 Other means of identification

Product number -
Other names 3H-Indazol-3-one

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:5686-93-1 SDS

5686-93-1Upstream product

5686-93-1Downstream Products

5686-93-1Relevant articles and documents

Electrosynthesis of cyclic α-carbonylazo compounds. Chemical stability of the electrogenerated dienophiles and in situ trapping of dienes

Lorans,Hurvois,Moinet

, p. 807 - 813 (2007/10/03)

Dienophilic cyclic α-carbonylazo compounds were prepared electrochemically by oxidation of the corresponding hydrazino compounds using a flow cell fitted with a graphite felt anode in acidic methanol or acetonitrile. The instability of these compounds in methanol was first studied. In situ Diels-Alder additions of these electrogenerated dienophiles and various dienes were performed in relatively good yields in acidic methanol or acetonitrile.

Heterocyclic agents

-

, (2008/06/13)

The invention concerns a 1,2-dihydro-3H-indazol-3-one derivative of formula I STR1 wherein Ra is hydrogen, halogeno, hydroxy, cyano, trifluoromethyl, 1-6C)alkyl or (1-6C)alkoxy; Rb is hydrogen or (1-6C)alkyl; Rc is hydrogen, (1-8C)alkyl or (3-8C)alkenyl;

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