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3-BROMO-5-IODOBENZOIC ACID

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3-BROMO-5-IODOBENZOIC ACID Basic information

Product Name:
3-BROMO-5-IODOBENZOIC ACID
Synonyms:
  • 3-BROMO-5-IODOBENZOIC ACID
  • 3-Bromo-5-idobenzoic acid
  • 3-BROMO-5-IODOBENZOIC ACID, 98+%
  • 3-BROMO-5-IODOBENZOI
  • 3-BroMo-5-iodobenzoic Acid, 97+%
  • 3-Bromine-5-Iodine Benzoic Acids
  • 3-Bromo-5-iodobenzoic Acid >
  • Benzoic acid, 3-bromo-5-iodo-
CAS:
188815-32-9
MF:
C7H4BrIO2
MW:
326.91
EINECS:
256-495-9
Product Categories:
  • Chemical Synthesis
  • Organic Building Blocks
  • intermediate
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Benzoic acid series
  • C7
  • Carbonyl Compounds
  • Carboxylic Acids
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
  • Acids & Esters
  • Bromine Compounds
  • Iodine Compounds
Mol File:
188815-32-9.mol
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3-BROMO-5-IODOBENZOIC ACID Chemical Properties

Melting point:
219-221 °C (lit.)
Boiling point:
385.2±37.0 °C(Predicted)
Density 
2.331±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in methanol. Sparingly Soluble (0.20 g/L) (25°C), Calc.
pka
3.46±0.10(Predicted)
form 
powder to crystal
color 
White to Light yellow to Light orange
Sensitive 
Light Sensitive
BRN 
3240837
InChI
InChI=1S/C7H4BrIO2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H,(H,10,11)
InChIKey
MKJBJYCBKXPQSY-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC(I)=CC(Br)=C1
CAS DataBase Reference
188815-32-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
29163990

MSDS

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3-BROMO-5-IODOBENZOIC ACID Usage And Synthesis

Chemical Properties

Solid

Uses

3-Bromo-5-iodobenzoic acid may be used in the preparation of the following: ? Phenyl(3-bromo-5-iodo)benzoate. ? As starting reagent for the large-scale synthesis of the thromboxane receptor antagonist 3-{3-[2-(4-chlorobenzenesulfonamido)ethyl]-5-(4-fluorobenzyl)phenyl}propionic acid, via regioselective Heck cross-coupling reaction. ? Methyl 3-bromo-5-iodobenzoate. ? 3-Bromo-5-(triisopropylsilylethynyl)benzoic acid, via Sonogashira coupling reaction. ? Trifluoroacetophenone.

General Description

3-Bromo-5-iodobenzoic acid (BrIBA) is a halogen substituted carboxylic acid.

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