25039-25-2

Basic information

• Product Name: 2-Propen-1-one, 1-phenyl-3-(phenylamino)-, (2Z)-
• Synonyms: (Z)-(2-anilino-vinyl) phenyl ketone;(Z) 3-Anilino-1-phenyl-2-propen-1-on;1-phenyl-3-(phenylamino)-2-propene-1-one;3-anilino-1-phenylprop-2-en-1-one;(Z)-1-phenyl-3-phenylamino-propenone
• CAS NO: 25039-25-2
• Molecular Formula: C15H13NO
• Molecular Weight: 223.274
• Mol File: 25039-25-2.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-phenyl-3-(phenylamino)-, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-phenyl-3-(phenylamino)-, (2Z)-(25039-25-2)
• EPA Substance Registry System: 2-Propen-1-one, 1-phenyl-3-(phenylamino)-, (2Z)-(25039-25-2)

Safety Data

• Hazardous Substances Data: 25039-25-2(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 3306-07-8 1-benzoyl-2-chloroethene 
• 15397-33-8 3-Oxo-3-phenylpropanal 
• 41125-10-4 benzoylacetaldehyde sodium salt 
• 142-04-1 aniline hydrochloride 
• 1131-80-2 (E)-3-(N,N-dimethylamino)-1-phenyl-2-propen-1-one 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 3623-15-2 phenyl propargyl ketone 
• 100-52-7 benzaldehyde 
• 93-55-0 1-phenyl-propan-1-one 
• 102-01-2 N-phenylacetoacetamide 
• 98-86-2 acetophenone 

Downstream Products

• 5220-59-7 1-(2-methyl-6-phenylpyridin-3-yl)ethan-1-one 
• 1166821-21-1 phenyl(4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methanone 
• 1166821-25-5 (4-(4-chlorophenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)(phenyl)methanone 
• 1166821-26-6 (4-(4-bromophenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)(phenyl)methanone 
• 1166821-22-2 4-(4-methylphenyl)-5-phenylmethanone-yl-3,4-dihydropyrimidine-2(1H)-thione 
• 64972-04-9 5-benzoyl-1-phenylpyridin-2(1H)-one 
• 1434474-81-3 (6-methyl-1,4,6-triphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone 
• 1434475-32-7 (6-methyl-4-phenethyl-1,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone 
• 1434475-41-8 (E)-(6-methyl-1,6-diphenyl-4-(2-phenylethylidene)-1,4,5,6-tetrahydropyridin-3-yl)(phenyl)methanone 
• 1434475-29-2 (4-butyl-6-methyl-1,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone 
• 1434475-38-3 (E)-(4-butylidene-6-methyl-1,6-diphenyl-1,4,5,6-tetrahydropyridin-3-yl)(phenyl)methanone 
• 1434475-26-9 (6-methyl-1,6-diphenyl-4-(p-tolyl)-1,6-dihydropyridin-3-yl)(phenyl)methanone 
• 1434475-23-6 C₃₁H₂₄FNO 
• 1434475-20-3 (6-cyclopropyl-1,4,6-triphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone 

Relevant articles and documents

X-RAY DIFFRACTION STUDY OF 1-BENZOYL-2-(N-ACETYL-N-PHENYLAMINO)ETHYLENE

An X-ray diffraction study has been carried out of the photochemically inactive 1-benzoyl-2-(N-acetyl-N-phenylamino)ethylene C17H15NO2 (diffractometer, λCuKα radiation, 1110 independent reflections, direct method, full-matrix least-squares method, R = 0.037).The crystals are monoclinic, a = 8.268(8), b = 9.703(4), c = 17.473(6) Angstroem, γ = 83 deg 20'(3'), space group P21/b, Z = 4.The possible reasons for the photostability of the compound related to the absence of steric strains in the molecule are discussed.

Fe-Catalyzed enaminone synthesis from ketones and amines

We have developed an iron-catalyzed direct olefination for enaminone synthesis, with saturated ketones as a source of olefins. This direct ketone β-functionalization reaction has readily available starting materials and a wide range of substrates and requires mild reaction conditions.

COMPOUNDS AND METHODS FOR HEMATOPOIETIC REGENERATION

The invention relates to compounds that promote hematopoietic regeneration. The invention further relates to methods of promoting hematopoietic regeneration using the novel compounds of the invention.