114787-91-6

Basic information

• Product Name: 4-METHOXY-3-METHYLBENZYL ALCOHOL
• Synonyms: RARECHEM AL BD 0539;4-METHOXY-3-METHYLBENZYL ALCOHOL;(4-Methoxy-3-methyl-phenyl)-methanol
• CAS NO: 114787-91-6
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.19
• Product Categories: Benzhydrols, Benzyl & Special Alcohols
• Mol File: 114787-91-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 258.3 °C at 760 mmHg
• Flash Point: 110.8 °C
• Appearance: /
• Density: 1.06 g/cm³
• Vapor Pressure: 0.00707mmHg at 25°C
• Refractive Index: 1.528
• PKA: 14.43±0.10(Predicted)
• CAS DataBase Reference: 4-METHOXY-3-METHYLBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXY-3-METHYLBENZYL ALCOHOL(114787-91-6)
• EPA Substance Registry System: 4-METHOXY-3-METHYLBENZYL ALCOHOL(114787-91-6)

Safety Data

• Hazardous Substances Data: 114787-91-6(Hazardous Substances Data)

Usage

General Description

4-Methoxy-3-methylbenzyl alcohol is a chemical compound with the molecular formula C9H12O2. It is a white solid at room temperature and is soluble in organic solvents. 4-METHOXY-3-METHYLBENZYL ALCOHOL is commonly used in the synthesis of various pharmaceuticals and as a starting material for the production of other chemicals. It is also used as a fragrance and flavoring agent in perfumes and food products. Additionally, 4-Methoxy-3-methylbenzyl alcohol has been studied for its potential pharmacological properties, including its ability to inhibit the growth of certain cancer cells. Overall, this chemical has a variety of industrial and medicinal applications.

InChI:InChI=1/C9H12O2/c1-7-5-8(6-10)3-4-9(7)11-2/h3-5,10H,6H2,1-2H3

Upstream product

• 60736-71-2 3-methyl-4-methoxybenzyl chloride 
• 127-09-3 sodium acetate 
• 32723-67-4 3-methyl-4-anisaldehyde 
• 14804-31-0 2-methyl-4-bromoanisole 
• 70347-04-5 4-Methoxy-3-methylbenzoesaeure-methylester 

Downstream Products

• 114787-92-7 3-(3-methyl-4-methoxyphenyl)methyl-N-BOC-histidine methyl ester 
• 1369423-32-4 diethyl 4-methoxy-3-methylbenzyl phosphate 
• 1260021-70-2 4-methoxy-3-methylbenzyl methanesulfonate 
• 102872-99-1 4-methoxy-3-methyl-benzaldehyde-semicarbazone 
• 32723-67-4 3-methyl-4-anisaldehyde 
• 6738-23-4 2,4-dimethylanisole 
• 144341-73-1 6-Methoxy-1,1,4a,7-tetramethyl-2-phenylsulfanyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthrene-9-carbonitrile 
• 144341-87-7 2-Benzenesulfinyl-6-methoxy-1,1,4a,7-tetramethyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 

Relevant articles and documents

PYRIMIDINE COMPOUNDS CONTAINING ACIDIC GROUPS

The present disclosure relates to a class of pyrimidine derivatives having immunomodulating properties that act via TLR7 which are useful in the treatment of viral infections and cancers.

Benzylic phosphates as electrophiles in the palladium-catalyzed asymmetric benzylation of azlactones

Palladium-catalyzed asymmetric benzylation has been demonstrated with azlactones as prochiral nucleophiles in the presence of chiral bisphosphine ligands. Benzylic electrophiles are utilized under two sets of reaction conditions to construct a new tetrasubstituted stereocenter. Electron density of the phenyl ring dictates the reaction conditions, including the leaving group. The reported methodology represents a novel asymmetric carbon-carbon bond formation in an amino acid precursor.

Imidazopyridinone derivatives and their use as phosphodiesterase inhibitors

A compound (Ia): wherein the variables are defined in the specification, its prodrug or a pharmaceutically acceptable salt thereof useful in the treatment of angina, hypertension etc.