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(3-Chloro-5-methoxyphenyl)methanol is an organic compound with the molecular formula C8H9ClO2, belonging to the class of phenols and phenolic compounds. It features a chlorine atom and a methoxy group attached to a phenyl ring, along with a hydroxyl group attached to a carbon atom, which imparts its phenolic properties. This versatile chemical is known for its potential use in various applications, including as a building block for the synthesis of pharmaceuticals and agrochemicals, as well as an intermediate in the production of various fine chemicals.

82477-68-7

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82477-68-7 Usage

Uses

Used in Pharmaceutical Industry:
(3-Chloro-5-methoxyphenyl)methanol is used as a building block for the synthesis of pharmaceuticals due to its unique structure and phenolic properties. It can be incorporated into the development of new drugs, potentially offering novel therapeutic options for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, (3-Chloro-5-methoxyphenyl)methanol serves as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties make it a valuable component in the development of effective and environmentally friendly agricultural products.
Used in Fine Chemicals Production:
(3-Chloro-5-methoxyphenyl)methanol is used as an intermediate in the production of various fine chemicals. Its versatility and unique structure allow it to be a key component in the synthesis of specialty chemicals used in a wide range of applications, from fragrances to dyes and other industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 82477-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,7 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82477-68:
(7*8)+(6*2)+(5*4)+(4*7)+(3*7)+(2*6)+(1*8)=157
157 % 10 = 7
So 82477-68-7 is a valid CAS Registry Number.

82477-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-CHLORO-5-METHOXYPHENYL)METHANOL

1.2 Other means of identification

Product number -
Other names Benzenemethanol,3-chloro-5-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:82477-68-7 SDS

82477-68-7Relevant academic research and scientific papers

IN VIVO IMAGING COMPOUNDS

-

, (2009/07/03)

The invention relates to a compound of formula (I) having use for in vivo imaging of the NR2B subtype of the NMDA receptor. [image]

Substituted Diphenylethers, -Amines, -Sulfides and -Methanes for the Treatment of Respiratory Disease

-

Page/Page column 23; 25, (2009/01/20)

The invention relates to substituted diphenylethers, -amines, -sulfides, and -methanes as useful pharmaceutical compounds for treating respiratory-disorders, pharmaceutical compositions containing them, and processes for their preparation.

NOVEL COMPOUNDS

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Page/Page column 40, (2008/06/13)

The invention relates to substituted phenylacetic acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.

Reaction of Some 1,4-Benzoquinone Mono-oximes with Methanolic Hydrogen Chloride

Sargent, Melvyn V.

, p. 1095 - 1098 (2007/10/02)

When 2-methyl-1,4-benzoquinone 4-oxime (1) reacted with methanolic hydrogen chloride at 25-30 deg C the product was 2-chloro-4,6-dimethoxy-3-methylaniline (2).Similarly 1,4-benzoquinone 4-oxime (7) gave 2-chloro-4,6-dimethoxyaniline (8), 3-methyl-1,4-benzoquinone 4-oxime (11) gave 2-chloro-4-methoxy-6-methoxymethylaniline (12) and 2-chloro-4-methoxy-6-methylaniline (13), and 2-methoxy-1,4-benzoquinone 4-oxime (19) gave 2-chloro-4,5-dimethoxyaniline (20).

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