1038726-89-4

Basic information

• Product Name: (2-chloro-6-methoxyphenyl)methanol
• Synonyms: (2-chloro-6-methoxyphenyl)methanol;2-chloro-6-methoxybenzenemethanol
• CAS NO: 1038726-89-4
• Molecular Formula: C₈H₉ClO₂
• Molecular Weight: 172.60886
• Mol File: 1038726-89-4.mol

Chemical Properties

• Boiling Point: 268.2±25.0 °C(Predicted)
• Appearance: /
• Density: 1.239±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 14.01±0.10(Predicted)
• CAS DataBase Reference: (2-chloro-6-methoxyphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-chloro-6-methoxyphenyl)methanol(1038726-89-4)
• EPA Substance Registry System: (2-chloro-6-methoxyphenyl)methanol(1038726-89-4)

Safety Data

• Hazardous Substances Data: 1038726-89-4(Hazardous Substances Data)

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.

Upstream product

• 936479-46-8 methyl 6-chloro-2-methoxybenzoate 
• 3260-89-7 2-chloro-6-methoxybenzoic acid 
• 54166-96-0 methyl 2-amino-6-methoxybenzoate 
• 29866-54-4 2-chloro-6-methoxybenzaldehyde 

Downstream Products

• 29866-54-4 2-chloro-6-methoxybenzaldehyde 
• 83781-95-7 2-(2-chloro-6-methoxyphenyl)acetonitrile 
• 18362-30-6 2-chloro-6-hydroxybenzaldehyde 
• 1154740-80-3 6-chloro-2H-chromene-3(4H)-one 

Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS FOR HISTONE LYSINE DEMETHYLASE INHIBITION

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

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

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

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

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

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

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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