62085-36-3

Basic information

• Product Name: (2E)-2-(4-chlorobenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• Synonyms: (2E)-2-(4-chlorobenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 62085-36-3
• Molecular Weight: 298.769
• Mol File: 62085-36-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2E)-2-(4-chlorobenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-2-(4-chlorobenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(62085-36-3)
• EPA Substance Registry System: (2E)-2-(4-chlorobenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(62085-36-3)

Safety Data

• Hazardous Substances Data: 62085-36-3(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 

Downstream Products

• 87384-15-4 1,2-trans-1-(p-(β-pyrrolidinoethoxy)phenyl)-2-(p-chlorobenzyl)-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-70-7 1,2-trans-1-(p-acetoxy)-2-(p-chlorobenzyl)-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-63-8 1-(o-hydroxyphenyl)-2-p-chlorobenzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-66-1 1-(p-hydroxyphenyl)-2-p-chlorobenzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 87384-05-2 2-p-chlorobenzyl-6-methoxy-1-tetralol 
• 62085-82-9 2-p-chlorobenzyl-6-methoxy-1-tetralone 

Relevant articles and documents

Synthesis, structure and antimicrobial evaluation of new 3,3a,4,5-tetrahydro-2H-benzo[g]indazol-2-yl-thiazol-4(5H)-ones

The reaction of semicarbazide or thiosemicarbazide with 2-arylidene-1-tetralones under alkaline condition affords 3,3a,4,5-tetrahydro- 2H-benzo[g]indazole-2-carbo(thio)amides as a mixture of cis and trans diastereoisomers of 3-H and 3a-H. The synthesis of

Studies in Antifertility Agents: Part XXVIII-1,2-trans-1-(p-(&β-Pyrrolidinoethoxy)phenyl)-2-substituted-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalenes

Substituted 2-benzyl-6-methoxy-1-tetralones (8-10), obtained by catalytic hydrogenation of 2-arylidene-1-tetralones (5-7), on NaBH4 reduction give a mixture of 1,2-trans-/cis-isomers of 2-benzyl-1-tetralols (11-13).Ac2O-pyridine treatment of 11 furnishes