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439-80-5

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439-80-5 Usage

Aromatic compound

Consists of a phenol group substituted with a fluorine atom and another phenyl group.

Uses

Commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds.

Antimicrobial properties

Inhibits the growth of various microorganisms, used in disinfectants and sanitizers.

Potential medical applications

Studied for its potential use in the treatment of certain diseases and conditions, of interest in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 439-80-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 439-80:
(5*4)+(4*3)+(3*9)+(2*8)+(1*0)=75
75 % 10 = 5
So 439-80-5 is a valid CAS Registry Number.

439-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-fluorophenyl)phenol

1.2 Other means of identification

Product number -
Other names 2'-Fluor-2-hydroxy-biphenyl

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:439-80-5 SDS

439-80-5Downstream Products

439-80-5Relevant articles and documents

Activation of Reducing Agents. Sodium Hydride Containing Complex Reducing Agents. 32. NiCRAL's as Very Efficient Agents in Promoting Cross-Coupling of Aryl Halides

Lourak, Mouhsine,Vanderesse, Regis,Fort, Yves,Caubere, Paul

, p. 4844 - 4848 (2007/10/02)

Nickel-containing complex reducing agents NiCRA-bpy are shown to be the first nickel reagents able to efficiently perform cross-coupling of aryl halides.The presence of KI in the reaction medium generally improves the procedure.The mechanism and influence of the structures of the substrates are discused.

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