213599-21-4

Basic information

• Product Name: Benzene, 1-(bromoethynyl)-2-iodo-
• CAS NO: 213599-21-4
• Molecular Formula: C8H4BrI
• Molecular Weight: 306.928
• Mol File: 213599-21-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(bromoethynyl)-2-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(bromoethynyl)-2-iodo-(213599-21-4)
• EPA Substance Registry System: Benzene, 1-(bromoethynyl)-2-iodo-(213599-21-4)

Safety Data

• Hazardous Substances Data: 213599-21-4(Hazardous Substances Data)

Upstream product

• 26260-02-6 2-iodobenzaldehyde 
• 265670-90-4 3,3-diethyl-1-(2-((trimethylsilyl)ethynyl)phenyl)triaz-1-ene 
• 265671-00-9 3,3-diethyl-1-(2-iodophenyl)triaz-1-ene 
• 137648-47-6 1-iodo-2-ethynylbenzene 
• 615-43-0 2-iodophenylamine 
• 766-50-7 (2-iodophenyl)-acetylene 
• 213599-20-3 1-(2,2-dibromovinyl)-2-iodobenzene 

Downstream Products

• 1056775-95-1 C₂₃H₁₆INO₂ 
• 1056775-53-1 C₁₇H₁₂INO₂ 

Relevant articles and documents

A sequential metal-catalyzed C-N bond formation in the synthesis of 2-amido-indoles

(Chemical Equation Presented) A sequential metal-catalyzed C-N bond formation employing ortho-haloaryl acetylenic bromides is described. The initial amidation is highly selective for C8P-N bond formation, leading to o-haloaryl-substiluted ynami

Synthesis of enantiopure estrone via a double heck reaction

A novel efficient catalytic approach to steroids by a double Heck reaction of the vinyl bromides 2 and the CD-building block 3 is presented. The new estrogen analogues 1a and 1b are formed via 23a and 23b in a highly regio- and stereoselective manner in g