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4-Bromobenzoyl chloride

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4-Bromobenzoyl chloride Basic information

Product Name:
4-Bromobenzoyl chloride
Synonyms:
  • 4-BroMobenzoyl Chloride, 97+%
  • The broMine benzoyl chloride
  • P-BROMOBENZOYL CHLORIDE
  • 4-BROMOBENZOYL CHLORIDE
  • AKOS BBS-00003926
  • 4-Brorobenzoylchloride
  • 4-Bromobenzoyl chlor
  • Of broMine chloride
CAS:
586-75-4
MF:
C7H4BrClO
MW:
219.46
EINECS:
209-580-1
Product Categories:
  • Pyridines ,Halogenated Heterocycles
  • Acid Halides
  • Absolute Configuration Determination (Exciton Chirality CD Method)
  • Analytical Chemistry
  • Carbonyl Compounds
  • Organic Building Blocks
  • Aromatic Halides (substituted)
  • Enantiomer Excess & Absolute Configuration Determination
  • Exciton Chirality CD Method (for Hydroxyl Groups)
  • K00001
Mol File:
586-75-4.mol
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4-Bromobenzoyl chloride Chemical Properties

Melting point:
36-39 °C(lit.)
Boiling point:
246 °C
Density 
1.6111 (rough estimate)
refractive index 
1.5963 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform, Methanol (Slightly)
form 
Low Melting Solid
color 
White to light brown
Water Solubility 
Soluble in methanol. Reacts with water forming Hcl.
Sensitive 
Moisture Sensitive
BRN 
636641
Stability:
Moisture Sensitive
CAS DataBase Reference
586-75-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzoyl chloride, 4-bromo-(586-75-4)
EPA Substance Registry System
Benzoyl chloride, 4-bromo- (586-75-4)
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Safety Information

Hazard Codes 
C
Risk Statements 
34-37
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
19-21
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29163900

MSDS

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4-Bromobenzoyl chloride Usage And Synthesis

Chemical Properties

White to light brown low melting solid

Uses

4-Bromobenzoyl chloride is used in the synthesis of HIV-1 protease inhibitors. It is also used in the synthesis of oxazoles, cyclohexanone derivatives as analgesic and antimicrobial agents.

Purification Methods

Check IR of a film to see if OH bands are present. If absent then recrystallise from pet ether and dry it in vacuo. If OH bands are weak, then distil it in vacuo and recrystallise if necessary. If OH bands are very strong, then treat with an equal volume of redistilled SOCl2 reflux for 2hours, then evaporate excess of SOCl2 and distil the residual oil or low melting solid. Store it in the dark away from moisture. LACHRYMATORY. [Martin & Partington J Chem Soc 1175 1936, Beilstein 9 IV 1023.]

4-Bromobenzoyl chloride Preparation Products And Raw materials

Preparation Products

4-Bromobenzoyl chlorideSupplier

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