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58585-01-6

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58585-01-6 Usage

Chemical Structure

Phenyl ring with a bromine atom attached to carbon at position 2
Acetophenone group with an amino group attached to carbon at position 2’

Physical Properties

Appearance: White to off-white solid
Odor: Mild, aromatic

Uses

Intermediate in pharmaceutical synthesis, particularly for anti-inflammatory and analgesic drugs
Synthesis of other organic compounds
Reagent in organic chemistry reactions

Biological Properties

Studied for potential antibacterial and antifungal properties
Subject of interest in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 58585-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58585-01:
(7*5)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*1)=156
156 % 10 = 6
So 58585-01-6 is a valid CAS Registry Number.

58585-01-6SDS

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 2-amino-1-(2-bromophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-Amino-phenacylbromid

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:58585-01-6 SDS

58585-01-6Relevant articles and documents

Synthesis of 2,3-disubstituted 4-oxoquinolines and 3-substituted fused 4-oxoquinolines

Alkhathlan, Hamad Z.,Al-Farhan, Khalid A.

, p. 641 - 655 (2007/10/03)

Seven 2,3-disubstituted 4-oxoquinolines were prepared via two methods. In the first one 2,3-disubstituted 4-oxoquinolines were prepared via the condensation of 2-amino-α-cyanoacetophenone with substituted phthalic anhydrides, while in the second method the fused isoindolo[2,1-a]quinolines and pyrrolo[1,2-a]quinolines were first prepared and then converted to 4-oxoquinolines. X-Ray crystal structure analysis of ethyl 2-[3-cyano-4-oxo-2-quinolyl]benzoate is reported.

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