70481-01-5

Upstream product

• 7462-70-6 4-chloro-1,3-diphenyl-but-2c-en-1-one 
• 532-27-4 1-chloroacetophenone 
• 54435-79-9 (E)-1,3-diphenyl-3-methyl-2-propen-1-one 

Downstream Products

• 7462-78-4 (+/-)-5t-chloromethyl-3,5c-diphenyl-4,5-dihydro-isoxazol-4r-ol 
• 860759-20-2 1,2,4-triphenyl-pyrrol-3-ol 
• 7462-78-4 (+/-)-5c-chloromethyl-3,5t-diphenyl-4,5-dihydro-isoxazol-4r-ol 
• 7462-77-3 (2RS,3RS)-4-chloro-2,3-epoxy-1,3-diphenyl-butan-1-one oxime 
• 1026-46-6 3,5-Diphenylpyridazine 
• 857419-10-4 3-chloro-1,2,4-triphenyl-pyrrole 
• 7462-77-3 (2RS,3SR)-4-chloro-2,3-epoxy-1,3-diphenyl-butan-1-one oxime 
• 3274-56-4 2,4-diphenylpyrrole 

Relevant academic research and scientific papers

Crystal structure of 3-chloromethyl-(3-phenyl-oxiranyl)phenyl methanone: New monoclinic polymorph

The compound, 3-chloromethyl-(3-phenyl-oxiranyl)phenyl methanone [m.f. C16H13O2Cl] was a self-condensation product of phenacyl chloride where the reaction carried out in ethanol medium using inorganic base. This was crystalized in monoclinic with space group P21/c (no. 14), a = 10.1312 (2) ?, b = 11.7728 ?, c = 11.8566 ?, V = 1344.07 ?3, Z = 4 and ρcalc. = 1.348 mg/mm3. The dihedral angle between two aromatic rings is 73.46 (5). The epoxide ring is oriented at dihedral angles of 62.12 (9°) and 60.87 (7°) with respect to the phenyl and benzoyl rings. The non-classical intermolecular hydrogen bonding of C-HO type has been observed in the crystal structure of molecule.