68120-35-4

Basic information

• Product Name: (3-BroMo-4-Methylphenyl)Methanol
• Synonyms: (3-BroMo-4-Methylphenyl)Methanol;3-Bromo-4-methylbenzenemethanol;3-Bromo-4-methylbenzyl alcohol;Benzenemethanol, 3-bromo-4-methyl-
• CAS NO: 68120-35-4
• Molecular Formula: C₈H₉BrO
• Molecular Weight: 201.06046
• Mol File: 68120-35-4.mol
• Article Data: 12

Chemical Properties

• Melting Point: 38-42°C
• Boiling Point: 283.4±25.0 °C(Predicted)
• Flash Point: >110℃
• Appearance: /
• Density: 1.481±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.29±0.10(Predicted)
• CAS DataBase Reference: (3-BroMo-4-Methylphenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-BroMo-4-Methylphenyl)Methanol(68120-35-4)
• EPA Substance Registry System: (3-BroMo-4-Methylphenyl)Methanol(68120-35-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 68120-35-4(Hazardous Substances Data)

Usage

General Description

(3-Bromo-4-Methylphenyl)Methanol, also known as BM-4-MP, is a chemical compound that belongs to the class of phenylmethanols. It is often used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. BM-4-MP has a bromine atom and a methyl group attached to the phenyl ring, giving it unique chemical properties that make it useful in a variety of applications. It is also used in the production of fragrances and flavors, as well as in the synthesis of other organic compounds. BM-4-MP is a versatile and important chemical compound with diverse industrial and scientific applications.

Upstream product

• 7697-26-9 3-bromo-4-methylbenzoic acid 
• 36276-24-1 3-bromo-4-methyl-benzaldehyde 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 72985-21-8 5-(hydroxymethyl)-2-methylbenzoic acid 
• 1260824-22-3 1,3-bis(3-bromo-4-methylphenyl)urea 
• 183723-09-3 3-bromo-4-methyl-benzamide 
• 72985-24-1 methyl 5-(hydroxymethyl )-2-methylbenzoate 
• 675148-96-6 methyl 5-formyl-2-methylbenzoate 
• 315188-34-2 5-(hydroxymethyl)-2-methylbenzonitrile 
• 105650-34-8 5-formyl-2-methylbenzoic acid 
• 1609540-80-8 (3-bromo-4-methylbenzyloxy)(tert-butyl)dimethylsilane 
• 1609540-87-5 tert-butyldimethyl((4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxy)silane 
• 1609540-83-1 5-(((tert-butyldimethylsilyl)oxy)methyl)-2-methylbenzaldehyde 
• 1609540-76-2 5-((tert-butyldimethylsilyloxy)methyl)-2-methylbenzoic acid 
• 1400755-04-5 [4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol 
• 1544739-90-3 (5aR,6S,6aS)-3-((3-(2-methoxypyridin-4-yl)-4-methylbenzyl)oxy)-5,5a,6,6a-tetrahydrocyclopropa[4,5]cyclopenta[1,2-c]pyridine-6-carboxylic acid 
• 1544739-93-6 (5aR,6S,6aS)-ethyl 3-((3-(2-methoxypyridin-4-yl)-4-methylbenzyl)oxy)-5,5a,6,6a-tetrahydrocyclopropa[4,5]cyclopenta[1,2-c]pyridine-6-carboxylate 

Relevant articles and documents

ANTIDIABETIC SUBSTITUTED HETEROARYL COMPOUNDS

The present invention relates to a compound represented by formula I: and pharmaceutically acceptable salts thereof. The compounds of formula I are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.

SPIRO-SUBSTITUTED OXINDOLE DERIVATIVES HAVING AMPK ACTIVITY

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

Synthesis of benzyl alcohol building blocks bearing an aldehyde, pinacol borane or carboxylic acid motif via lithium-bromide exchange

A range of useful disubstituted benzyl alcohol building blocks have been synthesised in multigram quantities in a lithium-bromide exchange to give aldehyde, carboxylic acid and pinacol -boranes in high yields. Georg Thieme Verlag Stuttgart · New York.