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1038726-89-4

(2-chloro-6-methoxyphenyl)methanol is a chemical compound with the molecular formula C8H9ClO2. It is a white to off-white solid that is commonly used in organic synthesis as a reagent for the preparation of various pharmaceutical and agrochemical products. It is also known for its use in the production of dyes and other chemical intermediates. Derived from phenol, (2-chloro-6-methoxyphenyl)methanol can be synthesized through a series of chemical reactions. Careful handling and storage are required, as it is considered harmful if absorbed through the skin or ingested, and it can cause irritation to the eyes and respiratory system.

1038726-89-4

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1038726-89-4 Usage

Uses

Used in Pharmaceutical Industry:
(2-chloro-6-methoxyphenyl)methanol is used as a reagent for the preparation of various pharmaceutical products due to its ability to be synthesized into a range of compounds with potential medicinal properties.
Used in Agrochemical Industry:
(2-chloro-6-methoxyphenyl)methanol is used as a reagent for the preparation of various agrochemical products, contributing to the development of effective substances for agricultural applications.
Used in Dye Production:
(2-chloro-6-methoxyphenyl)methanol is used as a chemical intermediate in the production of dyes, playing a role in the synthesis of colorants for various industries.
Used in Chemical Intermediates:
(2-chloro-6-methoxyphenyl)methanol is used as a building block in the synthesis of other chemical intermediates, which can be further processed or used in different chemical reactions to create a variety of end products.

Check Digit Verification of cas no

The CAS Registry Mumber 1038726-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,7,2 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1038726-89:
(9*1)+(8*0)+(7*3)+(6*8)+(5*7)+(4*2)+(3*6)+(2*8)+(1*9)=164
164 % 10 = 4
So 1038726-89-4 is a valid CAS Registry Number.

1038726-89-4SDS

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-Chloro-6-methoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names [2-chloro-6-(methyloxy)phenyl]methanol

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:1038726-89-4 SDS

1038726-89-4Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS FOR HISTONE LYSINE DEMETHYLASE INHIBITION

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Paragraph 0628; 0640, (2022/03/09)

The present disclosure relates generally to compounds and pharmaceutical compositions for the selective inhibition of histone lysine demethylase5 (KDM5), particularly KDM5B, and methods of their use in treating conditions and diseases associated with KDM5 activity.

Methanol as hydrogen source: Transfer hydrogenation of aromatic aldehydes with a rhodacycle

Aboo, Ahmed H.,Bennett, Elliot L.,Deeprose, Mark,Robertson, Craig M.,Iggo, Jonathan A.,Xiao, Jianliang

supporting information, p. 11805 - 11808 (2018/11/10)

A cyclometalated rhodium complex has been shown to perform highly selective and efficient reduction of aldehydes, deriving the hydrogen from methanol. With methanol as both the solvent and hydrogen donor under mild conditions and an open atmosphere, a wide range of aromatic aldehydes were reduced to the corresponding alcohols, without affecting other functional groups.

N-PYRAZOLYL CARBOXAMIDES AS CRAC CHANNEL INHIBITORS

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Page/Page column 58, (2010/11/05)

The present invention relates to amide compounds, processes for their preparation, pharmaceutical compositions containing these compounds and to their use in the treatment of disorders, conditions or disorders such as allergic disorders, inflammatory disorders and disorders of the immune system.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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, (2009/06/27)

Compounds of formula I : wherein c, R2, R3, R4, R5, R6, R7 and R8 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 72-73, (2009/06/27)

Compounds of formula (I): wherein R4, R6 and R7 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 81; 82, (2009/06/27)

Compounds of formula (I): wherein c, X, Y, R2, R4 and R5 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 78-79, (2009/06/27)

The present invention relates to compounds of formula (I) wherein c, X, Y, R2, R3, R4 and R6 are as defined herein, compositions and uses thereof for treating human immunodeficiency virus (HIV) infection. In particular, the present invention provides novel inhibitors of HIV integrase, pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HIV infection

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