21855-80-1

Basic information

• Product Name: 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether
• Synonyms: 4-(3,4-Dihydronaphthalen-1-yl)phenyl methyl ether; 4-(4-Methoxyphenyl)-1,2-dihydronaphthalene; naphthalene, 1,2-dihydro-4-(4-methoxyphenyl)-
• CAS NO: 21855-80-1
• Molecular Formula: C₁₇H₁₆O
• Molecular Weight: 236.3083
• EINECS: 606-847-8
• Mol File: 21855-80-1.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 360.9°C at 760 mmHg
• Flash Point: 144.2°C
• Density: 1.095g/cm³
• Vapor Pressure: 4.45E-05mmHg at 25°C
• Refractive Index: 1.599
• CAS DataBase Reference: 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether(21855-80-1)
• EPA Substance Registry System: 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether(21855-80-1)

Safety Data

• Hazardous Substances Data: 21855-80-1(Hazardous Substances Data)

Upstream product

• 79560-27-3 1-hydroxy-1-(4-methoxyphenyl)tetralin 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 104-15-4 toluene-4-sulfonic acid 
• 1072840-85-7 3,4-dihydronaphthalen-1-yl pivalate 
• 5720-07-0 4-methoxyphenylboronic acid 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 33397-21-6 tris(4-methoxyphenyl)bismuth 
• 149512-01-6 1,2-dihydro-4-iodonaphthalene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 1046113-15-8 7b-(4-methoxyphenyl)-1a,2,3,7b-tetrahydro-1-oxacyclopropa[a ]naphthalene 
• 117266-87-2 2-(p-anisoyl)phenylpropionic acid 
• 3771-17-3 4-(1,2,3,4-tetrahydro-1-naphthyl)-phenol 
• 79836-63-8 trans-N-methyl-4-(methoxyphenyl)-1,2,3,4-tetrahydro-1-naphthalenamine hydrochloride 
• 79560-05-7 cis-N-methyl-4-(methoxyphenyl)-1,2,3,4-tetrahydro-1-naphthalenamine hydrochloride 
• 79560-31-9 N-methyl-4-(4-methoxyphenyl)-1,2-dihydro-1-naphthalenamine hydrochloride 
• 79560-29-5 N-methyl-4-hydroxy-4-(4-methoxyphenyl)-1,2,3,4-tetrahydro-1-naphthalenamine 
• 79560-28-4 4-hydroxy-4-(4-methoxyphenyl)-1-tetralone 
• 19353-89-0 1-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene 
• 855409-38-0 4-(3,4-Dihydro-[1]naphthyl)-phenol 
• 27331-33-5 1-(4-methoxyphenyl)naphthalene 

Relevant articles and documents

Solid phase synthesizing method of dihydronaphthalene compound

A solid phase synthesizing method of a dihydronaphthalene compound I belongs to the field of organic chemistry and comprises: 1, using 1% crosslinked polystyrene resin as a carrier to prepare a polystyrene-loaded selenium base succinimide reagent III; 2, under catalyzing of fluoroform sulfonic acid trimethyl estersil, using the III to induce olefin V to be subjected to intramolecular cyclization to form 3-polystyrene-loaded selenium base-1,2,3,4-tetrahydronaphthalene VI; 3, removing VI by an oxidant through oxidation without further separating, thereby directly obtaining dihydronaphthalene I. Raw materials are easy to obtain, the product yield is good, the purity is high, the operation is simple and convenient, the posttreatment is simple and the method has well industrial application prospect.

Cu-catalyzed intramolecular hydroarylation of alkynes

An efficient Cu-catalyzed intramolecular hydroarylation reaction of alkynes has been developed. The reaction is accomplished under mild conditions and shows good tolerance to both electron-rich and electron-deficient aryl nucleophiles. A series of aryl, h

A one-pot preparation of aryl- and heteroarylcycloalkenes: Application to the total synthesis of (±)-laurokamurene B

A general one-pot method has been developed for the preparation of various aryl- and heteroarylcycloalkenes. After lithiation of aryl and heteroaryl bromides followed by transmetalation with CeCl3, the organocerium addition to cycloalkanones proceeds clea