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2891-30-7

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2891-30-7 Usage

Structure

A brominated derivative of 1,8-dihydroxyanthracen-9(10H)-one

Classification

Belongs to the group of anthraquinones

Applications

Widely used in the synthesis of various organic compounds and in medicinal chemistry as a building block for drug development

Biological and pharmacological activities

Exhibits potential biological and pharmacological activities, making it a valuable target for research in the pharmaceutical industry

Presence of bromine atom

Provides unique properties and reactivity

Utility

Useful in the development of new materials and biologically active compounds

Chemical properties

The bromine atom in the molecule can undergo various reactions such as substitution, elimination, and addition reactions, which can be exploited for the synthesis of new compounds

Check Digit Verification of cas no

The CAS Registry Mumber 2891-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2891-30:
(6*2)+(5*8)+(4*9)+(3*1)+(2*3)+(1*0)=97
97 % 10 = 7
So 2891-30-7 is a valid CAS Registry Number.

2891-30-7SDS

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 10-bromo-1,8-dihydroxy-10H-anthracen-9-one

1.2 Other means of identification

Product number -
Other names 10-bromo-1,8-dihydroxyanthracen-9(10h)-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:2891-30-7 SDS

2891-30-7Relevant articles and documents

Antipsoriatic anthrones with modulated redox properties. 3. 10-Thio- substituted 1,8-dihydroxy-9(10H)-anthracenones as inhibitors of keratinocyte growth, 5-lipoxygenase, and the formation of 12(S)-HETE in mouse epidermis

Müller, Klaus,Huang, Hsu-Shan,Wiegrebe, Wolfgang

, p. 3132 - 3138 (2007/10/03)

The synthesis of a series of 1,8-dihydroxy-9(10H)-anthracenones bearing sulfur-linked substituents in the 10-position is described. These compounds were evaluated for their ability to inhibit the growth of the human keratinocyte cell line HaCaT and the 5-

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