1032231-24-5

Basic information

• Product Name: 2-BROMO-5-IODOBENZALDEHYDE
• Synonyms: 2-BROMO-5-IODOBENZALDEHYDE
• CAS NO: 1032231-24-5
• Molecular Formula: C₇H₄BrIO
• Molecular Weight: 310.91
• Mol File: 1032231-24-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 105-107 °C(Solv: hexane (110-54-3))
• Boiling Point: 311.3±27.0 °C(Predicted)
• Appearance: /
• Density: 2.231±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• Solubility: Acetone (Slightly), Chloroform (Slightly)
• CAS DataBase Reference: 2-BROMO-5-IODOBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-5-IODOBENZALDEHYDE(1032231-24-5)
• EPA Substance Registry System: 2-BROMO-5-IODOBENZALDEHYDE(1032231-24-5)

Safety Data

• Hazardous Substances Data: 1032231-24-5(Hazardous Substances Data)

Usage

Uses

2-Bromo-5-iodobenzaldehyde is a useful reactant in organic synthesis.

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 289617-98-7 2?bromo-4?iodobromomethylbenzene 

Downstream Products

• 1378427-96-3 5-cyclopropyl-2-(4-fluorophenyl)-6-(N-(2-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yl)ethyl)methylsulfonamido)-N-methylbenzofuran-3-carboxamide 
• 1378465-81-6 6-(N-(3-((tert-butyldimethylsilyloxy)methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)methylsulfonamido)-5-cyclopropyl-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide 
• 1378431-50-5 6-(N-(4-bromo-3-((tert-butyldimethylsilyloxy)methyl)phenethyl)methylsulfonamido)-5-cyclopropyl-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide 
• 1378431-49-2 (2-bromo-5-(2-bromoethyl)benzyloxy)(tert-butyl)dimethylsilane 
• 1378431-48-1 2-(4-bromo-3-((tert-butyldimethylsilyloxy)methyl)phenyl)ethanol 
• 1378431-47-0 (5-allyl-2-bromobenzyloxy)(tert-butyl)dimethylsilane 
• 1378382-90-1 (2-bromo-5-iodobenzyloxy)(tert-butyl)dimethylsilane 
• 946525-30-0 4-bromo-3-hydroxymethyl-1-iodo-benzene 

Relevant articles and documents

Dibenzo[: B, e] phosphindolizines synthesized by a ring-closing metathesis of benzo [b] phospholes with two vinyl tethers

Dibenzo[b,e]phosphindolizines 1 were successfully synthesized by a ring-closing metathesis of benzo[b]phosphole chalcogenides 2a-2c with two vinyl tethers (for chalcogen analogs 1a-1c), and by a deselenization reaction (for lone-pair analog 1d). The structures, properties, and bowl inversion derived from a phosphorus atom were fully investigated.