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347-60-4

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347-60-4 Usage

Type of compound

Organic compound

Functional groups

Ketone, fluoro-substituted phenyl group, phenylethanone moiety

Aromatic characteristics

Yes

Ketone characteristics

Yes

Primary use

Pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceuticals

Additional use

Building block in the production of other organic compounds

Potential applications

Medical applications due to its chemical properties

Bioactivity

Considered a potential bioactive compound

Check Digit Verification of cas no

The CAS Registry Mumber 347-60-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 347-60:
(5*3)+(4*4)+(3*7)+(2*6)+(1*0)=64
64 % 10 = 4
So 347-60-4 is a valid CAS Registry Number.

347-60-4SDS

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 1-(3-fluoro-4-hydroxyphenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names 3-Fluor-4-dimethylamino-anilin

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:347-60-4 SDS

347-60-4Relevant articles and documents

An improved synthesis of hydroxy aryl ketones by fries rearrangement with methanesulfonic acid/methanesulfonic anhydride

Jeon, Ingyu,Mangion, Ian K.

experimental part, p. 1927 - 1930 (2012/10/08)

Methanesulfonic acid treated with methanesulfonic anhydride effectively mediates the Fries rearrangement of aryl esters to give hydroxy aryl ketones with high yields. Georg Thieme Verlag Stuttgart · New York.

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