1084789-69-4

Basic information

• Product Name: C₁₆H₁₆N₂*ClH
• Synonyms: C₁₆H₁₆N₂*ClH
• CAS NO: 1084789-69-4
• Molecular Weight: 272.777
• Mol File: 1084789-69-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₆N₂*ClH(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₆N₂*ClH(1084789-69-4)
• EPA Substance Registry System: C₁₆H₁₆N₂*ClH(1084789-69-4)

Safety Data

• Hazardous Substances Data: 1084789-69-4(Hazardous Substances Data)

Upstream product

• 10602-37-6 1,1,3,3-tetraethoxy-2-methyl-propane 
• 142-04-1 aniline hydrochloride 

Downstream Products

• 105688-80-0 α-methyl-β-anilinoacrolein 
• 612-58-8 3-methylquinoline 
• 56149-65-6 2-methyl-1-phenylamino-3-phenylimino-propene 

Relevant articles and documents

PREPARATION OF 3-SUBSTITUTED QUINOLINES. II. PREPARATION AND CYCLODEHYDRATION OF α-ALKYL- AND α-PHENYL-β-ARYLAMINOACROLEIN DERIVATIVES

α-Methyl-β-arylaminoacroleins were prepared by the hydrolysis of 2-methyl-1-arylamino-3-arylimino-1-propene derivatives. α-Ethyl- and α-phenyl-β-arylaminoacroleins were prepared by the reaction of arylamine and 2-substituted 1,1,3,3-tetraethoxypropane derivatives. 3-Methyl, 3-ethyl- and 3-phenylquinolines were obtained from α-methyl-, α-ethyl and α-phenyl-β-arylaminoacroleins on heating with aluminum bromide in good yields. α-Bromo-β-anilinoacrolein (9b) was prepared by the reaction of β-anilinoacrolein (6b) and N-bromosuccinimide.Reaction of 9b and aluminum bromide did not afford 3-bromoquinoline.