![]() 3-Chloropropiophenone structure
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Common Name | 3-Chloropropiophenone | ||
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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-Chloropropiophenone3-Chloropropiophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 3-Chloropropiophenone |
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Synonym | More Synonyms |
Description | 3-Chloropropiophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog | |
In Vitro | 3-氯苯丙酮是一种小分子化合物。 |
Density | 1.1±0.1 g/cm3 |
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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 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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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 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2914700090 |
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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% |
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, ... |
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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... |
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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)
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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 |