38119-08-3

Basic information

• Product Name: 3-BENZOYL-2-NAPHTHOIC ACID
• Synonyms: 3-BENZOYL-2-NAPHTHOIC ACID;3-Benzoyl-2-napthoicacid
• CAS NO: 38119-08-3
• Molecular Formula: C₁₈H₁₂O₃
• Molecular Weight: 276.29
• EINECS: 253-786-4
• Mol File: 38119-08-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 497.8°Cat760mmHg
• Flash Point: 269°C
• Appearance: /
• Density: 1.289g/cm³
• Vapor Pressure: 9.93E-11mmHg at 25°C
• Refractive Index: 1.678
• CAS DataBase Reference: 3-BENZOYL-2-NAPHTHOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BENZOYL-2-NAPHTHOIC ACID(38119-08-3)
• EPA Substance Registry System: 3-BENZOYL-2-NAPHTHOIC ACID(38119-08-3)

Safety Data

• Hazardous Substances Data: 38119-08-3(Hazardous Substances Data)

Usage

General Description

3-BENZOYL-2-NAPHTHOIC ACID is a chemical compound with the molecular formula C20H14O3. It is a derivative of naphthalene and is commonly used in organic synthesis as a starting material for the preparation of various organic compounds. 3-BENZOYL-2-NAPHTHOIC ACID has been studied for its potential applications in pharmaceuticals, particularly as an anti-inflammatory and anti-cancer agent. Additionally, it has been investigated for its use in the production of dyes and pigments. 3-BENZOYL-2-NAPHTHOIC ACID is a versatile compound with a range of potential uses in the fields of medicine, chemistry, and materials science.

InChI:InChI=1/C18H12O3/c19-17(12-6-2-1-3-7-12)15-10-13-8-4-5-9-14(13)11-16(15)18(20)21/h1-11H,(H,20,21)

Upstream product

• 6270-17-3 ethyl 3-benzoylpropanoate 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 71-43-2 benzene 
• 611-73-4 Benzoylformic acid 
• 93-09-4 naphthalene-2-carboxylate 
• 2051-95-8 succinylbenzene 
• 124-41-4 sodium methylate 
• 67-56-1 methanol 
• 716-39-2 2,3-Naphthalenedicarboxylic anhydride 
• 2169-87-1 naphthalene-2,3-dicarboxylic acid 

Downstream Products

• 1090-13-7 5,12-naphthacenequinone 
• 644-13-3 C₆H₅COC₁₀H₇ 
• 18929-62-9 naphthalene-2,3-diylbis(phenylmethanone) 
• 36724-38-6 1,4-Diphenylbenzophthalazin 
• 1260224-35-8 (R)-2-(1-phenylethyl)naphthalene 
• 627528-35-2 6,8,15,17-tetraphenylheptacene-7,16-quinone 
• 18929-61-8 1,3-dihydro-1,3-diphenylnaphtho[2,3-c]-furan-1-ol 
• 18929-57-2 1,3-diphenylnaphtho[2,3-c]furan 
• 18929-60-7 1,3-dihydro-3-phenylnaphtho[2,3-c]-furan-1-one 
• 856202-36-3 3-benzyl-[2]naphthoic acid 

Relevant articles and documents

Phenyl substituted pyridazine structure unit containing compounds and methods for their preparation and use

The invention discloses compounds containing phenyl substituted pyridazine structural unit, and a preparation method and application thereof. The structural general formula of the compounds containing phenyl substituted pyridazine structural unit is disclosed as Formula I. The compounds disclosed as Formula I have proper nuclear magnetic detection; and in order to solve the problems of less research on near-infrared materials and deficiency in high-efficiency high-stability near-infrared luminescent materials at present stage, the invention provides a series of near-infrared luminescent materials containing phenyl substituted pyridazine structure. The compounds have the advantages of accessible raw material, simple preparation process and high overall yield, and have important application value for researching development and application of near-infrared materials.

Synthesis and photophysical properties of dihydroheptacenes: New blue-emitting materials

7,16-Dihydroheptacenes (1-3) substituted at the 6, 8, 15, and 17 positions are synthesized as blue emitters potentially useful in organic light emitting diodes (OLEDs). The photophysical properties of 1-3 (λmax = 424-428 nm, ΦF = 0.15-0.21, τF = 2.35-2.67 ns in CH2Cl2) are discussed. They are shown to be stable and efficient blue emitters in the solid state (ΦF = 0.37-0.44). The X-ray crystal structure of 1 is reported.