73396-87-9

Basic information

• Product Name: Benzenamine, 2-iodo-N-2-propenyl-
• CAS NO: 73396-87-9
• Molecular Formula: C9H10IN
• Molecular Weight: 259.09
• Mol File: 73396-87-9.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-iodo-N-2-propenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-iodo-N-2-propenyl-(73396-87-9)
• EPA Substance Registry System: Benzenamine, 2-iodo-N-2-propenyl-(73396-87-9)

Safety Data

• Hazardous Substances Data: 73396-87-9(Hazardous Substances Data)

Upstream product

• 76464-99-8 N-benzyl-2-iodoaniline 
• 106-95-6 allyl bromide 
• 615-43-0 2-iodophenylamine 
• 107-18-6 allyl alcohol 

Downstream Products

• 130013-22-8 2-iodo-N-allyl-N-benzylaniline 
• 83-34-1 3-Methylindole 
• 130013-23-9 2-iodo-N-allyl-N-benzoylaniline 
• 73396-92-6 2-iodo-N,N-diallylaniline 
• 830-74-0 1-allyl-1H-indole-2,3-dione 
• 1006727-95-2 allyl(2-ethynylphenyl)amine 
• 1403587-57-4 C₁₃H₁₂INO 
• 130013-41-1 N-benzyl-3-((1-hydroxycyclohexyl)methyl)indoline 
• 130013-42-2 N-allyl-3-((1-hydroxycyclohexyl)methyl)indoline 

Relevant articles and documents

Insertion Reaction of 2-Halo- N -allylanilines with K 2S Involving Trisulfur Radical Anion: Synthesis of Benzothiazole Derivatives under Transition-Metal-Free Conditions

A synthesis of benzothiazole derivatives through the reaction of 2-halo- N -allylanilines with K 2S in DMF is developed. The trisulfur radical anion S 3· -, which is generated in situ from K 2S in DMF, initiates

A Palladium-Catalyzed Double Carbonylation Approach to Isatins from 2-Iodoanilines

A high-yielding procedure for the synthesis of isatins has been developed. Sequential Pd-catalyzed double carbonylation of 2-iodoanilines with near stoichiometric amounts of CO followed by acid-promoted cyclization readily affords an array of isatins. The conversion of 2-iodoanilines to isatins in good to excellent yields was found to proceed with good functional group tolerance. This protocol proved adaptable to 13C-isotope labeling of isatins, which was extended to the synthesis of the 13C-isotope labeled antiviral drug metisazone and the experimental anti-schizophrenia drug ML137.

Highly selective N-allylation of anilines under microwave irradiation

An easy and rapid procedure for the preparation of a variety of mono- and bis-allylated anilines via the reaction of allyl bromide with a wide range of anilines under microwave irradiation is described. This approach allows use of mild conditions and short reaction times to give high selectivities and excellent yields.