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117902-16-6

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117902-16-6 Usage

General Description

2-Fluoro-5-methoxyphenol is a chemical compound that falls under the category of organofluorines and phenols. As suggested by its name, its structure consists of a phenol group, a methoxy group (an oxygen bound to a methylene) attached to the 5th carbon, and a fluorine atom attached to the 2nd carbon. It is commonly used in the field of organic chemistry for various research and development purposes. Its chemical properties can be utilized for the synthesis of more complex chemical compounds. Like other phenols, it's essential to handle this chemical with proper safety measures due to its potential corrosiveness and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 117902-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,9,0 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117902-16:
(8*1)+(7*1)+(6*7)+(5*9)+(4*0)+(3*2)+(2*1)+(1*6)=116
116 % 10 = 6
So 117902-16-6 is a valid CAS Registry Number.

117902-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-5-methoxyphenol

1.2 Other means of identification

Product number -
Other names 2-fluoro-5-methoxyphenol

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:117902-16-6 SDS

117902-16-6Downstream Products

117902-16-6Relevant articles and documents

Derivatives of m-Guaiacol, Their Preparation and Their Uses

-

Paragraph 0125, (2021/11/05)

The invention concerns derivatives of m-guaiacol, their preparation and their uses as biocides, in particular as antibacterials or disinfectants.

A practical method for preparation of phenols from arylboronic acids catalyzed by iodopovidone in aqueous medium

Dong, Bin,Ke, Yanxiong,Lu, Guangying,Ren, Jiangmeng,Ren, Yaoyao,Zeng, Bu-Bing,Zhou, Bin

, (2019/09/06)

A novel and efficient strategy for the ipso-hydroxylation of arylboronic acids to phenols has been developed using inexpensive, readily available, air-stable water-soluble povidone iodine as catalyst and aqueous hydrogen peroxide as oxidizing agent. The reactions were performed at room temperature under metal-, ligand- and base-free condition in a short reaction time. The corresponding substituted phenols were obtained in moderate to good yields by oxidative hydroxylation of arylboronic acids in aqueous medium.

3,5-DISUBSTITUTED PYRAZOLES USEFUL AS CHECKPOINT KINASE 1 (CHK1) INHIBITORS, AND THEIR PREPARATIONS AND APPLICATIONS

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Paragraph 00091, (2018/02/28)

Potent inhibitors of Chk1 have the structure formula (I) below. Pharmaceutical compositions comprising the Chk1 inhibitors, uses thereof and their preparation process.

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