40662-66-6

Basic information

• Product Name: <α,α-2H2>-4-methylbenzyl alcohol
• Synonyms: <α,α-2H2>-4-methylbenzyl alcohol
• CAS NO: 40662-66-6
• Molecular Weight: 124.151
• Mol File: 40662-66-6.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: <α,α-2H2>-4-methylbenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: <α,α-2H2>-4-methylbenzyl alcohol(40662-66-6)
• EPA Substance Registry System: <α,α-2H2>-4-methylbenzyl alcohol(40662-66-6)

Safety Data

• Hazardous Substances Data: 40662-66-6(Hazardous Substances Data)

Upstream product

• 99-94-5 p-Toluic acid 
• 94-08-6 4-methylbenzoic acid ethyl ester 
• 99-75-2 4-methyl-benzoic acid methyl ester 
• 93-58-3 benzoic acid methyl ester 

Downstream Products

• 104-85-8 para-methylbenzonitrile 
• 1454775-18-8 C₁₈H₁₉⁽²⁾HN₂O 
• 32700-74-6 3-isopropyl-2-p-tolyl-3H-quinazolin-4-one 
• 1262758-64-4 N-(deuterio(4-methylphenyl)methylene)-4-methylbenzenesulfonamide 
• 156027-98-4 O-(α,α-dideuterio-p-methylbenzyl) N-acetoxybenzohydroxamate 
• 156028-05-6 O-(α,α-dideuterio-p-methylbenzyl) N-chlorobenzohydroxamate 
• 156028-03-4 α,α-dideuterio-p-methylbenzyl benzohydroxamate 
• 203579-68-4 2-methyl-5-trideuteriomethyl-1,4-benzoquinone 
• 26204-18-2 <α,α,α-2H3>p-xylene 
• 13277-99-1 4-methylbenzaldehyde-α-d₁ 
• 104-87-0 4-methyl-benzaldehyde 
• 57422-80-7 α,α-dideuterio-p-methylbenzyl bromide 
• 33712-36-6 <α,α-2H2>-4-methylbenzyl chloride 

Relevant articles and documents

Four-Component Radical Dual Difunctionalization (RDD) of Two Different Alkenes with Aldehydes and tert-Butyl Hydroperoxide (TBHP): An Easy Access to β,δ-Functionalized Ketones

A convenient Fe-catalyzed four-component radical dual difunctionalization and ordered assembly of two alkenes with aromatic/aliphatic aldehydes and TBHP to provide chain elongated β,δ-functionalized ketones via a one-pot procedure has been developed. Alde

An α, α - dideuterium substituted benzyl alcohol compound. Deuterated drug and method for reducing deuteration of benzoate compound

The invention relates to a method. Α, α-deuterated benzyl alcohol compound and preparation thereofΑ, αThe method for reducing and deuteration - dideuterium-substituted benzyl alcohol compounds is characterized in that the benzoate compound represented by

Photocatalysis with Quantum Dots and Visible Light: Selective and Efficient Oxidation of Alcohols to Carbonyl Compounds through a Radical Relay Process in Water

Selective oxidation of alcohols to aldehydes/ketones has been achieved with the help of 3-mercaptopropionic acid (MPA)-capped CdSe quantum dot (MPA-CdSe QD) and visible light. Visible-light-prompted electron-transfer reaction initiates the oxidation. The thiyl radical generated from the thiolate anion adsorbed on a CdSe QD plays a key role by abstracting the hydrogen atom from the C?H bond of the alcohol (R1CH(OH)R2). The reaction shows high efficiency, good functional group tolerance, and high site-selectivity in polyhydroxy compounds. The generality and selectivity reported here offer a new opportunity for further applications of QDs in organic transformations.