61161-21-5

Basic information

• Product Name: Benzene, 1-iodo-2-(1-methylethenyl)-
• Synonyms: 1-iodo-2-isopropenylbenzene;1-Iod-2-isopropenylbenzol;1-isopropenyl-2-iodo-benzene;1-Isopropenyl-2-jod-benzol
• CAS NO: 61161-21-5
• Molecular Formula: C9H9I
• Molecular Weight: 244.075
• Mol File: 61161-21-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, 1-iodo-2-(1-methylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-iodo-2-(1-methylethenyl)-(61161-21-5)
• EPA Substance Registry System: Benzene, 1-iodo-2-(1-methylethenyl)-(61161-21-5)

Safety Data

• Hazardous Substances Data: 61161-21-5(Hazardous Substances Data)

Upstream product

• 610-97-9 o-iodo-methyl-benzoic acid 
• 2142-70-3 2-iodoacetophenone 
• 7073-70-3 1-bromo-2-isopropenylbenzene 
• 2142-69-0 2-bromophenyl methyl ketone 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 69352-05-2 2-(2-iodophenyl)propan-2-ol 
• 88-67-5 2-Iodobenzoic acid 
• 444-29-1 2-iodo(trifluoromethyl)benzene 
• 75-24-1 trimethylaluminum 

Downstream Products

• 60997-84-4 Bis-(2-isopropenylphenyl)benzylalkohol 
• 6072-57-7 3-methylindanone 
• 60998-06-3 <α,αBis(2-isopropenylphenyl)benzyl>methylaether 
• 1313051-21-6 (S)-2-(2-iodophenyl)propan-1-ol acetate 
• 1313051-23-8 (R)-(-)-2-(2-iodophenyl)propan-1-ol acetate 
• 1313051-51-2 (R)-2-(2-iodophenyl)propan-1-ol 
• 1313051-53-4 (S)-2-(2-nitrophenyl)propan-1-ol 
• 1313051-25-0 C₁₁H₁₃NO₄ 
• 37778-99-7 (S)-2-phenyl-1-propanol 
• 1404432-64-9 2,3-bis(4-chlorophenyl)-1-(iodomethyl)-1-methyl-1H-indene 
• 1404432-65-0 2,3-bis(4-bromophenyl)-1-(iodomethyl)-1-methyl-1H-indene 
• 1404432-66-1 2,3-bis(3-fluorophenyl)-1-(iodomethyl)-1-methyl-1H-indene 
• 1404432-72-9 1-(iodomethyl)-2-(4-nitrophenyl)-1-methyl-3-(4-methoxyphenyl)-1H-indene 
• 1404432-73-0 1-(iodomethyl)-2-(4-methoxyphenyl)-1-methyl-3-(4-nitrophenyl)-1H-indene 

Relevant articles and documents

Chiral indole compounds and preparation method thereof

The invention discloses chiral indole compounds and a preparation method thereof. Cyclobutanone compounds with iodine-substituted benzene ring ortho-positions and aryl sulfonamide compounds with acetenyl-substituted benzene ring ortho-positions are used a

Taming Silylium Ions for Synthesis: N-Heterocycle Synthesis via Stereoselective C-C Bond Formation

Silylium ions (formally [R 3 Si] +) have long been the subject of investigations and significant debate in both theoretical and experimental chemistry, but few catalytic, synthetic applications have been reported due to the exception

Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons

A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropane 1,1-diesters has been successfully developed. This supplies an efficient and conceptually new strategy for construction of bridged bicyclo[2.2.2]octane skeletons. This [3 + 3]IMCC could be run up to gram scale and from easily prepared starting materials. This [3 + 3]IMCC, together with our previously reported [3 + 2]IMCC strategy, can afford either the bicyclo[2.2.2]octane or bicyclo[3.2.1]octane skeletons from the similar starting materials by regulating the substituents on vinyl group.