40638-92-4

Basic information

• Product Name: 1,1-dideuterio-2-phenylethanol
• Synonyms: 1,1-dideuterio-2-phenylethanol
• CAS NO: 40638-92-4
• Molecular Weight: 124.151
• Mol File: 40638-92-4.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1,1-dideuterio-2-phenylethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dideuterio-2-phenylethanol(40638-92-4)
• EPA Substance Registry System: 1,1-dideuterio-2-phenylethanol(40638-92-4)

Safety Data

• Hazardous Substances Data: 40638-92-4(Hazardous Substances Data)

Upstream product

• 122-78-1 phenylacetaldehyde 
• 536-74-3 phenylacetylene 
• 103-82-2 phenylacetic acid 
• 101-41-7 benzeneacetic acid methyl ester 
• 101-97-3 Ethyl 2-phenylethanoate 

Downstream Products

• 1390620-64-0 1,1,3,3-tetradeutero-2,3-diphenylpropan-1-ol 
• 54845-21-5 (3-bromopropyl-2,2-d₂)benzene 
• 17428-98-7 2-[D₂]-3-phenylpropan-1-ol 
• 29372-33-6 α,α-dideuterated hydrocinnamaldehyde 
• 66255-92-3 rac-(β,β-²H₂)styrene oxide 
• 66997-34-0 2-phenylethyldimethylamine-1,1-d2 oxide 
• 66997-32-8 2-phenylethyldimethylamine-1,1-d2 
• 19136-97-1 α-dideuterated 3-phenyl propionic acid 
• 60468-24-8 (2-deuterio-2-propenyl)benzene 

Relevant articles and documents

Isotopic Labeling Studies of the Thermal Rearrangement of Phenyloxirane to Phenylethanal

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Nickel-Catalyzed Electrochemical Reductive Relay Cross-Coupling of Alkyl Halides to Aryl Halides

A highly regioselective Ni-catalyzed electrochemical reductive relay cross-coupling between an aryl halide and an alkyl halide has been developed in an undivided cell. Various functional groups are tolerated under these mild reaction conditions, which pro

A Method for Bischler-Napieralski-Type Synthesis of 3,4-Dihydroisoquinolines

A new method for the Bischler-Napieralski-type synthesis of 3,4-dihydroisoquinolines was developed by a Tf2O-promoted tandem annulation from phenylethanols and nitriles. Its success was mainly due to the fact that a phenonium ion was formed in the process and practically functioned as a stable and reactive primary phenylethyl carbocation.