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HomeProduct name list2-Bromo-3'-chloropropiophenone

2-Bromo-3'-chloropropiophenone

  • CAS NO.:34911-51-8
  • Empirical Formula: C9H8BrClO
  • Molecular Weight: 247.52
  • MDL number: MFCD03701150
  • EINECS: 252-282-1
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-09-25 14:54:50
2-Bromo-3'-chloropropiophenone Structural

What is 2-Bromo-3'-chloropropiophenone?

Chemical properties

Yellow Oil

The Uses of 2-Bromo-3'-chloropropiophenone

It used as an important intermediate for raw material and intermediate used in organic synthesis agrochemical, pharmaceutical and dyestuff field.

Definition

2-Bromo-3'-chloropropiophenone (BCP), a yellow oil, is an intermediate used in the synthesis of bupropion and is also found as an impurity of bupropion hydrochloride. Bupropion is a second-generation antidepressant that was originally approved by the United States Food and Drug Administration (FDA) in 1985. It is a norepinephrine and dopamine transporter inhibitor and an antagonist at neuronal nicotinic acetylcholine receptors. Bupropion is also approved for smoking cessation[1].

Safety

The current United States Pharmacopeia (USP) specification is for no more than 0.1% BCP in the bupropion hydrochloride monograph. The Material Safety Data Sheet from a manufacturer indicates that BCP is irritating to the eyes, respiratory system, and skin. 2-Bromo-3'-chloropropiophenone was mutagenic with S9 metabolic activation, increasing the mutant frequencies in a concentration-dependent manner, up to 22- and 145-fold induction over the controls in Salmonella strains TA100 and TA1535, respectively. BCP was also positive in the in vitro micronucleus assay, resulting in up to 3.3- and 5.1-fold increase of micronucleus frequency for treatments in the absence and presence of S9, respectively; and 9.9- and 7.4-fold increase of aneuploidies without and with S9, respectively. The addition of N-acetyl-l-cysteine, an antioxidant, reduced the genotoxicity of BCP in both assays. Further studies showed that BCP treatment resulted in induction of reactive oxygen species (ROS) in the TK6 cells. The results suggest that BCP is mutagenic, clastogenic, and aneugenic, and that these activities are mediated via generation of reactive metabolites[1].

References

[1] Meng, Fanxue , et al. "Genotoxicity of 2-bromo-3′-chloropropiophenone." Toxicology & Applied Pharmacology 270.2(2013):158-163.

Properties of 2-Bromo-3'-chloropropiophenone

Boiling point: 148-148.5 °C(Press: 9 Torr)
Density  1.532
refractive index  1.5770
storage temp.  Refrigerator, Under Inert Atmosphere
solubility  Soluble in acetonitrile, chloroform, dichloromethane and ethyl acetate.
form  Liquid
color  Colorless to pale yellow
InChI InChI=1S/C9H8BrClO/c1-6(10)9(12)7-3-2-4-8(11)5-7/h2-6H,1H3
CAS DataBase Reference 34911-51-8(CAS DataBase Reference)

Safety information for 2-Bromo-3'-chloropropiophenone

Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405:Store locked up.

Computed Descriptors for 2-Bromo-3'-chloropropiophenone

InChIKey OFNMQTRHMBQQEA-UHFFFAOYSA-N
SMILES C(C1=CC=CC(Cl)=C1)(=O)C(Br)C

Abamectin manufacturer

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