648439-19-4

Basic information

• Product Name: (3-broMo-5-Methylphenyl)Methanol
• Synonyms: (3-broMo-5-Methylphenyl)Methanol;3-Bromo-5-methylbenzylalcohol;3-bromo-5-methylbenzyl alchol
• CAS NO: 648439-19-4
• Molecular Formula: C₈H₉BrO
• Molecular Weight: 201.07
• Mol File: 648439-19-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (3-broMo-5-Methylphenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-broMo-5-Methylphenyl)Methanol(648439-19-4)
• EPA Substance Registry System: (3-broMo-5-Methylphenyl)Methanol(648439-19-4)

Safety Data

• Hazardous Substances Data: 648439-19-4(Hazardous Substances Data)

Usage

General Description

(3-bromo-5-methylphenyl)methanol is a chemical compound that consists of a benzene ring with a bromine atom located at the 3rd position and a methyl group at the 5th position. The molecule also contains a hydroxyl group (-OH) attached to the carbon atom adjacent to the benzene ring. (3-broMo-5-Methylphenyl)Methanol is used in organic synthesis and can be utilized as a building block for the synthesis of various pharmaceuticals and agrochemicals. It is also used in the production of fragrances and other specialty chemicals. The compound's structure and functional groups make it a versatile intermediate in the manufacturing of a wide range of products.

Upstream product

• 1611-92-3 3-bromo-5-methylbenzaldehyde 
• 556-96-7 5-bromo-1,3-xylene 

Downstream Products

• 1611-92-3 3-bromo-5-methylbenzaldehyde 
• 1056893-13-0 C₈H₈BrCl 
• 1177558-71-2 tert-butyl (3-bromo-5-cyanobenzyl)carbamate 
• 1177558-50-7 3-(aminomethyl)-5-bromobenzonitrile 
• 1177558-49-4 3-bromo-5-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]benzonitrile 
• 124289-24-3 α-Bromo-3-bromo-5-cyanotoluene 
• 1007578-82-6 3-bromo-5-methylbenzamide 
• 124289-21-0 3-bromo-5-methylbenzonitrile 
• 58530-13-5 3-bromo-5-methyl-benzoic acid 

Relevant articles and documents

Method for preparation of aromatic alcohol by photocatalysis of aromatic aldehyde conversion

The invention relates to a method for preparation of aromatic alcohol by photocatalysis of aromatic aldehyde conversion. By means of a photocatalyst, under the conditions of illumination and inert gas, fatty alcohol is adopted as a proton donor for reduction reaction on aromatic aldehyde to obtain corresponding aromatic alcohol. Fatty alcohol is used as the proton donor, and light energy is used as the energy source to promote high-conversion-rate and high-selectivity synthesis of a series of aromatic alcohol compounds from aromatic aldehyde, the method has universal applicability, and is expected to realize industrial production; and the reaction process is green and environment-friendly, low in cost, easy to operate, short in reaction period, high in conversion rate and good in selectivity.

PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

The present invention relates to 2-pyridone derivatives of Formula (I) or (IV) as herein described, compositions containing such compounds, synthetic processes for making such compounds, and therapeutic methods that include the administration of such comp