119450-03-2

Basic information

• Product Name: 2,3-DIBROMO-3-(2-BROMOPHENYL)PROPIONIC ACID
• Synonyms: 2,3-dibromo-3-(2-bromophenyl)propanoic acid
• CAS NO: 119450-03-2
• Molecular Formula: C₉H₇Br₃O₂
• Molecular Weight: 386.86
• Product Categories: Aromatics Compounds;Aromatics
• Mol File: 119450-03-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 376.4°C at 760 mmHg
• Flash Point: 181.5°C
• Appearance: /
• Density: 2.184g/cm³
• Vapor Pressure: 2.46E-06mmHg at 25°C
• Refractive Index: 1.656
• PKA: 2.16±0.16(Predicted)
• CAS DataBase Reference: 2,3-DIBROMO-3-(2-BROMOPHENYL)PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIBROMO-3-(2-BROMOPHENYL)PROPIONIC ACID(119450-03-2)
• EPA Substance Registry System: 2,3-DIBROMO-3-(2-BROMOPHENYL)PROPIONIC ACID(119450-03-2)

Safety Data

• Hazardous Substances Data: 119450-03-2(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Powder

InChI:InChI=1/C9H7Br3O2/c10-6-4-2-1-3-5(6)7(11)8(12)9(13)14/h1-4,7-8H,(H,13,14)

Upstream product

• 7345-79-1 2-bromocinnamic acid 
• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 121263-08-9 (2-bromo-benzylidene)-malonic acid 
• 7345-79-1 2-bromocinnamic acid 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 246876-11-9 1-phenyl-2-trimethylsilyl-1-benzophosphepine 1-oxide 
• 154467-44-4 (Z,Z)-1-bromo-4-(2-bromophenyl)-1-trimethylsilyl-1,3-butadiene 
• 154081-41-1 1-phenyl-1-benzoarsepine 
• 154467-46-6 5-Phenyl-6-trimethylsilanyl-5H-5-arsa-benzocycloheptene 
• 154467-45-5 5-Phenyl-6-trimethylsilanyl-5H-5-phospha-benzocycloheptene 
• 154467-43-3 (Z)-1-(o-bromophenyl)-4-trimethylsilyl-1-buten-3-yne 
• 137072-83-4 1-phenyl-1-benzophosphepine 
• 153140-75-1 1-bromo-2-[(Z)-2-bromoethenyl]benzene 

Relevant articles and documents

Carbene-catalyzed LUMO activation of alkyne esters for access to functional pyridines

A carbene-catalyzed LUMO activation of α,β-unsaturated alkyne esters is reported. This catalytic process allows for effective reactions of alkyne esters with enamides to synthesize functional pyridines via simple protocols. A previously unexplored unsaturated alkyne acyl azolium intermediate is involved in the key step of the reaction.