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7-aminoquinoline-5,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64636-91-5

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64636-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64636-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64636-91:
(7*6)+(6*4)+(5*6)+(4*3)+(3*6)+(2*9)+(1*1)=145
145 % 10 = 5
So 64636-91-5 is a valid CAS Registry Number.

64636-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-aminoquinoline-5,8-dione

1.2 Other means of identification

Product number -
Other names 7-amino-quinoline-5,8-dione

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:64636-91-5 SDS

64636-91-5Upstream product

64636-91-5Downstream Products

64636-91-5Relevant academic research and scientific papers

Synthesis of 1,5- and 1,8-diazaanthraquinones by reaction of aminoquinolinequinones with β-dielectrophiles

Marcos, Alicia,Pedregal, Carmen,Avendano, Carmen

, p. 1763 - 1774 (1995)

Easily obtained amino derivatives of quinoline-5,8-quinone (1 and 2) and 4-methyl-(1H)2,5,8-quinolinetrione (3) react with β-dielectrophiles, affording aminoalkylidenemalonates in a convenient procedure. These compounds cyclise thermally to 1,5-diaza-(1H)4,9,10-anthracenetriones (10 and 19), 1,8-diaza-(1H)4,9,10-anthracenetriones (11 and 20) and 1,5-diaza-(1H, 5H)2,8,9,10-anthracenetetraones (12 and 21). The strategy is less convenient when applied to aromatic precursors. Knorr cyclisation of β-oxoanilides fails in both systems.

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