109519-45-1

Basic information

• Product Name: C₃₅H₂₉ClN₃O₃P
• Synonyms: C₃₅H₂₉ClN₃O₃P
• CAS NO: 109519-45-1
• Molecular Weight: 606.06
• Mol File: 109519-45-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₅H₂₉ClN₃O₃P(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₅H₂₉ClN₃O₃P(109519-45-1)
• EPA Substance Registry System: C₃₅H₂₉ClN₃O₃P(109519-45-1)

Safety Data

• Hazardous Substances Data: 109519-45-1(Hazardous Substances Data)

Upstream product

• 28889-23-8 Ethyl 2-benzoyl-4-chlorphenylazo-chloracetat 
• 109519-62-2 C₁₇H₁₄ClN₅O₃ 
• 603-35-0 triphenylphosphine 

Downstream Products

• 109519-57-5 7-Chloro-5-hydroxy-4,5-diphenyl-4,5-dihydro-[1,2,4]triazolo[1,5-a]quinazoline-2-carboxylic acid ethyl ester 
• 1016-78-0 3-chlorobenzophenone 
• 133031-98-8 7-Chloro-5-phenyl-1H-benzo[f][1,2,4]triazepine-3-carboxylic acid ethyl ester 
• 133032-03-8 1-(2-Benzoyl-4-chloro-phenyl)-1H-[1,2,4]triazole-3-carboxylic acid ethyl ester 

Relevant articles and documents

Reaction of C-(Triphenylphosphinimido)hydrazones with Isocyanates as a Route to 5-Arylamino- and 5-Alkylamino-1H-1,2,4-triazoles

Treatment of C-(triphenylphosphinimido)hydrazone (1) with aryl and alkyl isocyanates results in 5-arylamino- and 5-alkylamino-1H-1,2,4-triazoles (5), often accompanied by a minor quantity of the triazol-5-one (7).The related ortho-acyl-substituted substrates (8) react with phenyl isocyanate to give triazoloquinazolines (12) or (13) through the intermediacy of aminotriazoles (11).