Basic information Safety Supplier Related

4-BROMO-2-CHLOROACETANILIDE

Basic information Safety Supplier Related

4-BROMO-2-CHLOROACETANILIDE Basic information

Product Name:
4-BROMO-2-CHLOROACETANILIDE
Synonyms:
  • SALOR-INT L168270-1EA
  • 4-BROMO-2-CHLOROACETANILIDE
  • 4-Bromo-2-chloroacetanilide, 98+%
  • 4'-Bromo-2'-chloro-N-phenylacetamide
  • BUTTPARK 83\07-60
  • 4'-Bromo-2'-chloroacetanilide >
  • Acetamide, N-(4-bromo-2-chlorophenyl)-
  • 2-chloro-4-bromo acetanillide
CAS:
3460-23-9
MF:
C8H7BrClNO
MW:
248.5
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Anilines, Amides & Amines
  • Bromine Compounds
  • Chlorine Compounds
Mol File:
3460-23-9.mol
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4-BROMO-2-CHLOROACETANILIDE Chemical Properties

Melting point:
151-152°C
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in hot methanol (very faint turbidity).
form 
powder to crystal
color 
White to Light yellow
BRN 
2719133
CAS DataBase Reference
3460-23-9
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-37
HS Code 
2924297099

MSDS

  • Language:English Provider:ALFA
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4-BROMO-2-CHLOROACETANILIDE Usage And Synthesis

Uses

It is employed as a intermediate for pharmaceutical.

Synthesis

533-17-5

3460-23-9

General procedure for the synthesis of 4-bromo-2-chloro-N-acetylaniline from N-(2-chlorophenyl)acetamide: 1. HBr (40% aqueous, 0.08 mL, 0.55 mmol) was added to a stirred suspension of N-(2-chlorophenyl)acetamide (75 mg, 0.5 mmol) and Selectfluor (213 mg, 0.6 mmol) in water (3.0 mL). 2. the mixture was stirred at room temperature for 5 minutes until the ingredients were completely consumed (monitored by TLC). 3. Upon completion of the reaction, the reaction was quenched with saturated Na2S2O3 aqueous solution (2.0 mL) and water (20.0 mL). 4. The organic phase was extracted three times with CH2Cl2 (10.0 mL) and combined. 5. After evaporation of the solvent, the residue obtained was purified by silica gel column chromatography (eluent: petroleum ether-ethyl acetate=6:1, v/v) to afford 4-bromo-2-chloro-N-acetylaniline as a white solid (108 mg, 95% yield).

References

[1] Chemistry - A European Journal, 2017, vol. 23, # 5, p. 1044 - 1047
[2] Tetrahedron Letters, 2016, vol. 57, # 48, p. 5390 - 5394
[3] Journal of Chemical Research, Synopses, 1997, # 11, p. 432 - 433
[4] European Journal of Organic Chemistry, 2018, vol. 2018, # 43, p. 5972 - 5979
[5] Gazzetta Chimica Italiana, 1908, vol. 38 II, p. 22

4-BROMO-2-CHLOROACETANILIDE Preparation Products And Raw materials

Raw materials

4-BROMO-2-CHLOROACETANILIDESupplier

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