93655-02-8

Basic information

• Product Name: methyl 2-(naphthalen-1-yl)benzoate
• CAS NO: 93655-02-8
• Molecular Formula: C₁₈H₁₄O₂
• Molecular Weight: 262.3026
• Mol File: 93655-02-8.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 415.1°C at 760 mmHg
• Flash Point: 188.7°C
• Density: 1.156g/cm³
• Vapor Pressure: 4.24E-07mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: methyl 2-(naphthalen-1-yl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(naphthalen-1-yl)benzoate(93655-02-8)
• EPA Substance Registry System: methyl 2-(naphthalen-1-yl)benzoate(93655-02-8)

Safety Data

• Hazardous Substances Data: 93655-02-8(Hazardous Substances Data)

Upstream product

• 91-20-3 naphthalene 
• 134-20-3 2-carbomethoxyaniline 
• 88-65-3 2-bromobenzoic-acid 
• 610-96-8 methyl chlorobenzoate 
• 13922-41-3 1-Naphthylboronic acid 
• 610-94-6 2-bromobenzoic acid methyl ester 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 630-95-5 1-naphthyldiphenylmethanol 

Downstream Products

• 108981-92-6 2-(naphthalene-1-yl)benzoic acid 
• 569673-92-3 2-[2-(1-naphthyl)phenyl]-2-propanol 
• 1637660-36-6 5,9-dibromobenzo[c]fluoren-7-one 
• 1246940-13-5 (7,7-dimethyl-7H-benzo[c]fluorene-5-yl)boronic acid 
• 1356175-00-2 C₄₃H₃₁NS 
• 1121748-44-4 5-phenylamino-7,7-dimethyl-7H-benzo[c]fluorene 
• 954137-48-5 5- bromo-7,7-dimethyl-7H-benzo[c]fluorene 
• 112486-09-6 7,7-Dimethyl-7H-benzo[c]fluorene 
• 119438-34-5 3-(2-methoxycarbonyl-phenyl)-3-[1]naphthyl-acrylic acid tert-butyl ester 
• 111936-97-1 3-(2-carboxy-phenyl)-3-[1]naphthyl-acrylic acid 
• 118659-78-2 2-(2-tert-butoxycarbonyl-1-[1]naphthyl-vinyl)-benzoic acid 

Relevant articles and documents

Non-c2-symmetric bis-benzimidazolium salt applied in the synthesis of sterically hindered biaryls

A novel non-C2-symmetric bis-benzimidazolium salt derived from (±)-valinol has been prepared by a simple and straightforward process in good yield. The structure of bis-benzimidazolium salt provided a bulky steric group on the ethylene bridge; which facilitates the catalytic efficacy in the C(sp2 )–C(sp2 ) formation. Its catalytic activity in Suzuki–Miyaura cross-coupling reaction of unactivated aryl chlorides has been found to have high efficacy in 1 mol% Pd loading. This protocol demonstrated the potential on the synthesis of sterically hindered biaryls.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME

The present invention is an organic light emitting compound characterized by an aromatic amine derivative represented by chemical formula A. The aromatic amine derivative has excellent light emitting properties such as brightness, luminous efficiency, etc

Visible-Light-Induced Arene C(sp 2)-H Lactonization Promoted by DDQ and tert -Butyl Nitrite

A visible-light photocatalytic aerobic oxidative lactonization of arene C(sp 2)-H bonds proceeds in the presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and tert -butyl nitrite (TBN). Under the optimized conditions, a range of 2-arylbenzoic acids is converted into the corresponding benzocoumarin derivatives in moderate to excellent yields. This method is characterized by its atom economy, mild reaction conditions, the use of a green oxidant and metal-free catalysis.