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2-FLUORO-3-METHYLPHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77772-72-6

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77772-72-6 Usage

Chemical Properties

light yellow powder

Check Digit Verification of cas no

The CAS Registry Mumber 77772-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,7 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77772-72:
(7*7)+(6*7)+(5*7)+(4*7)+(3*2)+(2*7)+(1*2)=176
176 % 10 = 6
So 77772-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7FO/c1-5-3-2-4-6(9)7(5)8/h2-4,9H,1H3

77772-72-6SDS

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-Fluoro-3-methylphenol

1.2 Other means of identification

Product number -
Other names 2-FLUORO-3-METHYLPHENOL

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:77772-72-6 SDS

77772-72-6Relevant academic research and scientific papers

Selective Synthesis of Fluorophenol Derivatives

Takemoto, Ichiki,Yamasaki, Kaori

, p. 594 - 595 (2007/10/02)

The selective synthesis of fluorophenol derivatives starting from tert-butylphenol derivatives and fluorinating reagents is described. tert-Butylfluorophenol derivatives were treated with an aluminum chloride catalyst in toluene to afford the fluorophenol derivatives.

DIRECT FLUORINATION OF PHENOL AND CRESOLS

Misaki, Susumu

, p. 159 - 172 (2007/10/02)

A study has been made of the reaction of phenol with elemental fluorine using a variety of solvents and reaction temperatures.Yields of o- and p-fluorophenol were obtained as high as 85percent.The isomer ratio changed drastically between phenol conversions of 10percent and 56percent.The o-isomer changed to unidentified polymeric substances at higher conversion, but it might also be assumed that interconversion of some isomers is occuring.The three cresols have also been succesfully fluorinated with elemental fluorine. p-Cresol gave some expected 2-fluoroderivative but also formed a fluorocyclohexadienyl ketone.

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