3-Chloropropiophenone

Modify Date: 2025-08-20 18:44:29

3-Chloropropiophenone Structure
3-Chloropropiophenone structure
Common Name 3-Chloropropiophenone
CAS Number 936-59-4 Molecular Weight 168.62
Density 1.1±0.1 g/cm3 Boiling Point 263.3±23.0 °C at 760 mmHg
Molecular Formula C9H9ClO Melting Point 48-50 °C(lit.)
MSDS USA Flash Point 127.0±13.7 °C

 Use of 3-Chloropropiophenone


3-Chloropropiophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 3-Chloropropiophenone
Synonym More Synonyms

 3-Chloropropiophenone Biological Activity

Description 3-Chloropropiophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro 3-氯苯丙酮是一种小分子化合物。

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 263.3±23.0 °C at 760 mmHg
Melting Point 48-50 °C(lit.)
Molecular Formula C9H9ClO
Molecular Weight 168.62
Flash Point 127.0±13.7 °C
Exact Mass 168.034195
PSA 17.07000
LogP 2.23
Vapour Pressure 0.0±0.5 mmHg at 25°C
Index of Refraction 1.527
Stability Stable. Incompatible with strong bases, strong oxidizing agents.
Water Solubility Insoluble

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S37/39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2914700090

 Synthetic Route

 Customs

HS Code 2914700090
Summary HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

 Articles3

More Articles
Synthesis of enantiopure glycidol derivatives via a one-pot two-step enzymatic cascade.

Org. Biomol. Chem. 13(7) , 2146-52, (2015)

Styrene monooxygenase (SMO) can catalyze the kinetic resolution of secondary allylic alcohols to provide enantiopure glycidol derivatives. To overcome the low theoretical yield of kinetic resolution, ...

Asymmetric reduction of (S)-3-chloro-1-phenylpropanol from 3-chloropropiophenone by preheated immobilized Candida utilis.

Biotechnol. Lett. 31(12) , 1879-83, (2009)

An efficient method for asymmetric reduction of (S)-3-chloro-1-phenylpropanol from 3-chloropropiophenone was developed using preheated Candida utilis cells immobilized in calcium alginate gel beads. H...

Asymmetric Synthesis of (R)-Fluoxetine: A Practical Approach Using Recyclable and in-situ Generated Oxazaborolidine Catalyst. Padiya K, et al.

Chin. J. Chem. 27(6) , 1137-40, (2009)

 Synonyms

B-CHLOROPROPIOPHENONE
ω-Chloropropiophenone
3-Chloro-1-phenylpropan-1-one
3-chloro-1-phenyl-propan-1-one
Beta-Chloropropiophenone
3-Chloropropanophenone
β-Chloropropiophenone
EINECS 213-317-6
β-Chloroethyl phenyl ketone
3-Chloropropiophenone
3-Chloro-1-phenyl-1-propanone
2-Chloro-1-benzoylethane
Propiophenone, 3-chloro-
Propiophenone,3-chloro
PhCOCH2CH2Cl
1-Propanone, 3-chloro-1-phenyl-
MFCD00000990
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