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2-chloro-4-hydrazinyl-6,7-dimethoxyquinazoline hydrate (2:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37562-23-5

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37562-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37562-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,6 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37562-23:
(7*3)+(6*7)+(5*5)+(4*6)+(3*2)+(2*2)+(1*3)=125
125 % 10 = 5
So 37562-23-5 is a valid CAS Registry Number.

37562-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-chloro-6,7-dimethoxyquinazolin-4-yl)hydrazine,hydrate

1.2 Other means of identification

Product number -
Other names 2-Chloro-6,7-dimethoxy-4-hydrazinoquinazoline hemihydrate

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:37562-23-5 SDS

37562-23-5Relevant academic research and scientific papers

FUSED HETEROCYCLIC COMPOUNDS

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Page/Page column 90; 91, (2008/06/13)

This invention provides fused heterocyclic compounds, pharmaceutical compositions of the compounds, and methods of using the compounds for the treatment of, inter alia, IL-12 related disease and disorders.

Tricyclic 1,2,4-triazolo-quinazolines

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, (2008/06/13)

The invention discloses 5-substituted-1,2,4-triazolo[4,3-c]quinazolines and 1,2,4-triazolo[1,5-c]quinazolines having pharmacological activity in animals and useful, for example, as hypotensive and anti-inflammatory agents. The compounds may be prepared, for example, by reacting a 5-halo-1,2,4-triazolo-quinazoline with a compound representing the function to be introduced at the 5-position. The 5-halo-1,2,4-triazolo[4,3-c]quinazolines also have pharmacological activity, e.g., hypotensive and anti-inflammatory activity, and may be prepared by reacting a 4-hydrazino-quinazoline with trimethoxy methane. The 5-halo-1,2,4-triazolo[1,5-c]quinazolines also have hypotensive and anti-inflammatory activity and are prepared from the corresponding 1,2,4-triazolo-[1,5-c]quinazolin-5(1H)-one using phosphorus oxychloride, the quinazolin-5(1H)-one being in turn prepared from the 5-halo-1,2,4-triazolo[4,3-c]quinazoline.

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