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163190-79-2

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163190-79-2 Usage

General Description

(2-Bromo-4-methoxy-phenyl)methanol is an organic chemical compound that contains a bromine atom, a methoxy group, and a hydroxyl group attached to a benzene ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. The presence of the bromine atom makes it a useful intermediate in the preparation of specialty chemicals, and it can also be utilized as a reagent in organic chemistry reactions. Additionally, it has been investigated for its potential use as an antimicrobial agent due to its structural properties. Overall, (2-Bromo-4-methoxy-phenyl)methanol has versatile applications in the field of organic synthesis and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 163190-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,1,9 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 163190-79:
(8*1)+(7*6)+(6*3)+(5*1)+(4*9)+(3*0)+(2*7)+(1*9)=132
132 % 10 = 2
So 163190-79-2 is a valid CAS Registry Number.

163190-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-4-methoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,2-bromo-4-methoxy

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:163190-79-2 SDS

163190-79-2Relevant articles and documents

COMPOUNDS

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Page/Page column 121, (2020/01/24)

A compound of formula (I), or a pharmaceutically acceptable salt thereof.

Stereoselective Convergent Synthesis of Tetrahydro-5 H-benzo[c]fluorene via Nine-Membered Ring-Closing Metathesis and Transannular Acid-Mediated Cyclization/Nucleophilic Addition

Lekky, Anek,Ruengsatra, Tanachote,Ruchirawat, Somsak,Ploypradith, Poonsakdi

, p. 5277 - 5291 (2019/05/10)

The diene methyl ethers or acetates, constructed from the Li-Br exchange/addition reactions of 2-vinylbenzaldehydes and 2-(but-3-en-1-yl)bromoarenes followed by etherification or acetylation of the corresponding alcohols, smoothly underwent the ring-closi

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