110451-90-6

Basic information

• Product Name: (2-Bromo-5-methoxy-3-methylphenyl)methanol
• Synonyms: (2-Bromo-5-methoxy-3-methylphenyl)methanol
• CAS NO: 110451-90-6
• Molecular Formula: C₉H₁₁BrO₂
• Molecular Weight: 231.1
• Mol File: 110451-90-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-Bromo-5-methoxy-3-methylphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Bromo-5-methoxy-3-methylphenyl)methanol(110451-90-6)
• EPA Substance Registry System: (2-Bromo-5-methoxy-3-methylphenyl)methanol(110451-90-6)

Safety Data

• Hazardous Substances Data: 110451-90-6(Hazardous Substances Data)

Usage

General Description

(2-Bromo-5-methoxy-3-methylphenyl)methanol is a chemical compound with the molecular formula C9H11BrO2. It is a white solid and is used in various organic synthesis processes. (2-Bromo-5-methoxy-3-methylphenyl)methanol is often used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It has been studied for its potential biological activities, including its antimicrobial and anti-inflammatory properties. Additionally, it has been used as a building block in the synthesis of complex organic molecules. Overall, (2-Bromo-5-methoxy-3-methylphenyl)methanol is a versatile and useful compound in various chemical applications.

Upstream product

• 108-68-9 3,5-Dimethylphenol 
• 6267-34-1 2-bromo-5-methoxy-1,3-dimethyl-benzene 
• 874-63-5 3,5-dimethylmethoxybenzene 
• 164513-49-9 2-bromo-1-(bromomethyl)-5-methoxy-3-methylbenzene 
• 94742-92-4 methyl 2-bromo-5-methoxy-3-methylbenzoate 

Downstream Products

• 202195-07-1 3-methoxy-5-methyl-2-(1,4,5-trimethoxynaphthalen-2-yl)benzaldehyde 
• 199612-65-2 2-iodo-3-methoxy-5-methylbenzaldehyde 
• 119650-45-2 (2-iodo-3-methoxy-5-methylphenyl)methanol 
• 119650-44-1 (3-methoxy-5-methylphenyl)methanol 
• 7414-92-8 Tetrangulol 
• 1362209-16-2 2-bromo-5-methoxy-1-methyl-3-vinylbenzene 
• 1308649-72-0 2-bromo-5-methoxy-3-methylbenzaldehyde 
• 631910-75-3 (2-bromo-5-methoxy-3-methyl-benzyloxy)-acetic acid tert-butyl ester 
• 174417-54-0 2-bromo-5-methoxy-3-methylbenzoic acid 
• 207287-39-6 (S)-2-(2-Bromo-5-methoxy-3-methyl-phenyl)-4-isopropyl-4,5-dihydro-oxazole 
• 94742-92-4 methyl 2-bromo-5-methoxy-3-methylbenzoate 

Relevant articles and documents

New 2,2′-substituted 4,4′-dimethoxy-6,6′-dimethyl[1, 1′-biphenyls], inducing a strong helical twisting power in liquid crystals

Based on the stabilisation of the molecular motion by the chiral residue, novel optically active biphenylic chiral dopants for nematic liquid crystals were developed. This molecular congestion was obtained by introducing mesogenic residues on the 2,2′-positions of the chiral biphenyl; this led to a novel molecular architecture that was found to be efficient. The synthesised optically active biphenyls were characterised with very short cholesteric pitches when used as chiral dopants in nematic liquid crystals. The synthesis of the enatiomerically pure biphenyl dopants and their preliminary physicochemical characterisations are described.

Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

A New Family of Enantiomerically Pure Smectic C* Liquid Crystals with a Bridged Chiral Biphenyl Core

The synthesis of enantiomerically pure bridged biphenyl compounds, (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e] thiepine, 13, and (-)-(R)-3,9-bis(4-(dodecyloxy)benzoyloxy)-5,7-dihydro-1,11-dimethyldibenzo[c,e]- thiepin d