6552-64-3

Basic information

• Product Name: 3-(4-methoxyphenyl)-1-(4-phenylphenyl)prop-2-en-1-one
• Synonyms: 3-(4-methoxyphenyl)-1-(4-phenylphenyl)prop-2-en-1-one
• CAS NO: 6552-64-3
• Molecular Formula: C₂₂H₁₈O₂
• Molecular Weight: 314.38
• Mol File: 6552-64-3.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 509°C at 760 mmHg
• Flash Point: 224.4°C
• Appearance: /
• Density: 1.126g/cm³
• Vapor Pressure: 1.76E-10mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 3-(4-methoxyphenyl)-1-(4-phenylphenyl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)-1-(4-phenylphenyl)prop-2-en-1-one(6552-64-3)
• EPA Substance Registry System: 3-(4-methoxyphenyl)-1-(4-phenylphenyl)prop-2-en-1-one(6552-64-3)

Safety Data

• Hazardous Substances Data: 6552-64-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C22H18O2/c1-24-21-14-7-17(8-15-21)9-16-22(23)20-12-10-19(11-13-20)18-5-3-2-4-6-18/h2-16H,1H3

Upstream product

• 92-91-1 biphenyl-4-acetaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 92-52-4 biphenyl 
• 99-90-1 para-bromoacetophenone 
• 98-80-6 phenylboronic acid 

Downstream Products

• 76288-00-1 3-Biphenyl-4-yl-5-(4-methoxy-phenyl)-isoxazole 
• 76287-96-2 3-Biphenyl-4-yl-5-(4-methoxy-phenyl)-4,5-dihydro-isoxazole 
• 1017240-37-7 3-Biphenyl-4-yl-5-(4-methoxy-phenyl)-4,5-dihydro-1H-pyrazole 
• 30313-30-5 4-Biphenyl-4-yl-6-(4-methoxy-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester 
• 861406-40-8 C₂₆H₂₅N₃O₂ 
• 30314-06-8 3-Biphenyl-4-yl-5-(4-methoxy-phenyl)-cyclohex-2-enone 
• 77153-40-3 (cis)-1-p-biphenylyl-2-(p-methoxyphenyl)cyclopropane 
• 77153-41-4 (trans)-1-p-biphenylyl-2-(p-methoxyphenyl)cyclopropane 
• 51813-18-4 3-(biphenyl-4-yl)-5-(4-methoxyphenyl)pyrazole 
• 50497-96-6 4,5-dihydro-1-phenyl-3-diphenyl-5-(4-methoxyphenyl)-1H-pyrazole 

Relevant articles and documents

Synthesis of new schiff base of 1,3-oxazine and 1,3-thiazine derivatives derived from 4-phenyl substituted chalcones and evaluation of their antibacterial activity

Oxazine and thiazine heterocycles have distinctive interests due to their important class of natural and non-natural products and exhibit high biological activities in the pharmaceutical and biological fields. This work was planned to synthesize Schiff ba

Synthesis and characterization of 2-phenylpyrazoline derivatives and evaluation of their activities against antimicrobial and breast cancer cell line in vitro and in silico studies

The new series of 2-phenylpyrazoline derivatives (2a-j) were synthesized and evaluated for their antimicrobial, in silico and in vitro anticancer activity was performed by MTT assay using MDA-MB-231 (human breast adenocarcinoma) cell line. The 2-phenylpyr

Synthesis and characterization of 2-pyrazoline derivatives and their in silico and in vitro studies on antimicrobial and anticancer activities

The new series of 1-(4,5-dihydro-5-phenyl-3-diphenylpyrazol-1-yl)butan-1-one derivatives were synthesized by cyclization method using biphenyl chalcone with n-butyric acid and hydrazine hydrate. The synthesized 1-(4,5-dihydro-5-phenyl-3-diphenylpyrazol-1-