58536-96-2

Basic information

• Product Name: 2-allylamino-1-<(4-fluorophenyl)methyl>pyrido<2,3-d>pyrimidine-4(1H)-one
• Synonyms: 2-allylamino-1-<(4-fluorophenyl)methyl>pyrido<2,3-d>pyrimidine-4(1H)-one
• CAS NO: 58536-96-2
• Molecular Weight: 310.331
• Mol File: 58536-96-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-allylamino-1-<(4-fluorophenyl)methyl>pyrido<2,3-d>pyrimidine-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-allylamino-1-<(4-fluorophenyl)methyl>pyrido<2,3-d>pyrimidine-4(1H)-one(58536-96-2)
• EPA Substance Registry System: 2-allylamino-1-<(4-fluorophenyl)methyl>pyrido<2,3-d>pyrimidine-4(1H)-one(58536-96-2)

Safety Data

• Hazardous Substances Data: 58536-96-2(Hazardous Substances Data)

Upstream product

• 459-46-1 4-Fluorobenzyl bromide 
• 140-75-0 para-fluorobenzylamine 
• 21038-63-1 3-azaisatoic anhydride 
• 97484-91-8 2-<(4-fluorophenyl)methylamino>-3-pyridinecarboxylic acid 
• 2942-59-8 2-chloronicotinic acid 

Relevant articles and documents

The Chemistry of 3-Azaisatoic Anhydrides. Synthesis and Reactions of Polyaza Heterocycles

The preparation of a variety of N-substituted 3-azaisotoic anhydrides 3 and 8 is described.These anhydrides reacted with thiopseudoureas to give interesting bicyclic, tricyclic, and tetracyclic heterocycles many of which are new ring systems.One such hete

1-Substituted-2-disubstitutedamino-pyrido[2,3-D]pyrimidin-4(1H)-ones

Anti-histaminics of the formula SPC1 Wherein R1 is alkyl, alkenyl or phenalkyl, R2 and R3 are alkyl or alkenyl and R' is optional are prepared by alkylating or alkenylating a 1-substituted-2-monosubstituted-amino pyrido 2,