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7364-26-3

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7364-26-3 Usage

General Description

3-HYDROXY-5-METHYL (1H)INDAZOLE is a chemical compound with the molecular formula C9H8N2O. It belongs to the indazole family and is a derivative of indole. 3-HYDROXY-5-METHYL (1H)INDAZOLE has a hydroxy (OH) group and a methyl (CH3) group attached to the indazole ring, and is commonly used in organic synthesis and medicinal chemistry. It has potential pharmacological properties and is being researched for its potential use in drug development. 3-HYDROXY-5-METHYL (1H)INDAZOLE has also been studied for its antimicrobial and anti-cancer properties, making it an important compound in the field of pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 7364-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7364-26:
(6*7)+(5*3)+(4*6)+(3*4)+(2*2)+(1*6)=103
103 % 10 = 3
So 7364-26-3 is a valid CAS Registry Number.

7364-26-3SDS

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 5-methyl-1,2-dihydroindazol-3-one

1.2 Other means of identification

Product number -
Other names 5-methyl-1,2-dihydro-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:7364-26-3 SDS

7364-26-3Upstream product

7364-26-3Relevant articles and documents

Practical synthesis of 3-carboxyindazoles

Johnson, Barry L.,Rodgers, James D.

, p. 2681 - 2684 (2005)

A clean, high-yielding synthetic route to methyl 5-(bromomethyl)-1- tritylindazole 3-carboxylate 1 was needed. A principal intermediate was 5-methyl-3-carboxyindazole 2. An analysis of a by-product found after executing Schad's 3-carboxyindazole synthesis led to undertaking this reaction with an inverse addition in the principal step. This simple modification gave 2 in excellent and reproducible yields. Copyright Taylor & Francis, Inc.

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