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77282-37-2

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77282-37-2 Usage

Classification

Acridine derivative (heterocyclic compound containing nitrogen and oxygen atoms within a fused ring system)

Utilization

Organic synthesis and medicinal chemistry

Pharmaceutical applications

Antimicrobial and antitumor properties

Common use

Intermediate or building block in the production of other organic compounds

Distinctive properties

Fluorescent properties

Applications

Laboratory and research applications

Interest

Scientists and researchers in the chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 77282-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77282-37:
(7*7)+(6*7)+(5*2)+(4*8)+(3*2)+(2*3)+(1*7)=152
152 % 10 = 2
So 77282-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H8BrNO3/c1-19-14-10(15)13(18)11-8(12(14)17)6-7-4-2-3-5-9(7)16-11/h2-6H,1H3

77282-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2-methoxyacridine-1,4-dione

1.2 Other means of identification

Product number -
Other names 1,4-Acridinedione,3-bromo-2-methoxy

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:77282-37-2 SDS

77282-37-2Downstream Products

77282-37-2Relevant articles and documents

Heterocyclic quinones. I. 1,4-Acridinediones: potential antitumoral agents

Renault,Giorgi-Renault,Mailliet,et al.

, p. 24 - 34 (2007/10/02)

The authors investigate the synthesis of several 1,4-acridinediones substituted in position 2 or 2 and 3 simultaneously. These acridinediones are related to streptonigrin, the antitumor activity of which results from the redox properties of the 7-amino-6-methoxy-5,8-quinolinedione nucleus. Pacridinediones are particularly cytotoxic in vitro against the leukemia L1210 cell, but none of them shows antitumor activity in the L1210 tumor affected mouse.

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