118806-82-9

Basic information

• Product Name: 3-o-chlorophenyl-1-tetralone
• Synonyms: 3-o-chlorophenyl-1-tetralone
• CAS NO: 118806-82-9
• Molecular Weight: 256.732
• Mol File: 118806-82-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-o-chlorophenyl-1-tetralone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-o-chlorophenyl-1-tetralone(118806-82-9)
• EPA Substance Registry System: 3-o-chlorophenyl-1-tetralone(118806-82-9)

Safety Data

• Hazardous Substances Data: 118806-82-9(Hazardous Substances Data)

Upstream product

• 118806-79-4 3-o-chlorophenyl-4-phenylbutyric acid 
• 716-43-8 dimethyl homophthalate 
• 24393-51-9 ethyl 3-(2-chlorophenyl)acrylate 
• 22360-36-7 3-o-chlorophenyl-2-carboxy-4-phenylbutyric acid 
• 6768-20-3 diethyl 2-chlorobenzylidene malonate 
• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 121511-09-9 3-(2-Chloro-phenyl)-3,4-dihydro-2H-naphthalen-1-one oxime 
• 121511-13-5 3-(2-Chloro-phenyl)-naphthalen-1-ylamine 

Relevant articles and documents

Origin of stereocontrol in guanidine-bisurea bifunctional organocatalyst that promotes α-hydroxylation of tetralone-derived β-ketoesters: Asymmetric synthesis of β- And γ-substituted tetralone derivatives via organocatalytic oxidative kinetic resolution

The mechanism of asymmetric α-hydroxylation of tetralone-derived β-ketoesters with guanidine-bisurea bifunctional organocatalyst in the presence of cumene hydroperoxide (CHP) was examined by means of DFT calculations to understand the origin of the stereo