3-Chloropropiophenone

Names

[ CAS No. ]:
936-59-4

[ Name ]:
3-Chloropropiophenone

[Synonym ]:
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

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]:

Research Areas >> Others

[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

MSDS

Click to get detail MSDS

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

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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%

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)