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183709

Sigma-Aldrich

2′-Chloroacetophenone

97%

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About This Item

Formula condensata:
ClC6H4COCH3
Numero CAS:
2142-68-9
Peso molecolare:
154.59
Beilstein:
1858916
Numero CE:
218-397-6
Numero MDL:
MFCD00000560
Codice UNSPSC:
12352100
ID PubChem:
24851071
NACRES:
NA.22

Livello qualitativo

100

Saggio

97%

Forma fisica

liquid

P. eboll.

227-230 °C

Densità

1.190 g/mL at 20 °C

Gruppo funzionale

chloro
ketone

Stringa SMILE

CC(=O)c1ccccc1Cl

InChI

1S/C8H7ClO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3
ZDOYHCIRUPHUHN-UHFFFAOYSA-N

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Descrizione generale

2′-Chloroacetophenone undergoes stereoselective reduction to (R)-2′-chloro-1-phenyl-ethanol by Saccharomyces cerevisiae B5. It is commonly used as lacrimator.

Applicazioni

2′-Chloroacetophenone was employed as model substrate to investigate the enzymatic performance of Aspergillus terreus and Rhizopus oryzae in enantioselective bioreductions using glycerol as a co-solvent.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

190.4 °F

Punto d’infiammabilità (°C)

88 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
STBJ9651
STBG6991
STBD1735V
STBB6539V
STBC1960V

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K E Ferslew et al.
Journal of forensic sciences, 31(2), 658-665 (1986-04-01)
2-Chloroacetophenone (CN) and o-chlorobenzylidene malononitrile (CS) are the most common chemical agents used as lacrimators in the United States. There is a lack of complete spectral data on these compounds in the literature. Spectral data (ultraviolet, fluorescence, proton nuclear magnetic
Hui Song et al.
Journal of chromatographic science, 57(4), 299-304 (2019-02-06)
The synthetic condition of tulobuterol was optimized to gain lower impurity content. Two intermediates were analyzed, and three degradation impurities were isolated using preparative liquid chromatography for the first time and subsequently characterized by various techniques. Possible degradation impurities were
Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent.
Andrade LH, et al.
Tetrahedron Asymmetry, 20(13), 1521-1525 (2009)
Zhi-Min Ou et al.
Sheng wu gong cheng xue bao = Chinese journal of biotechnology, 19(2), 206-211 (2005-06-22)
(R)-chlorprenaline, a selective activator of beta2 receptor and an effective drug for bronchitis and asthma, is industrially prepared from (R)-2'-chloro-1-phenyl-ethanol. In this communication, we describe (1) the identification of Saccharomyces cerevisiae B5 as an effective host for stereoselective reduction of
Kunpeng Li et al.
Scientific reports, 7(1), 3081-3081 (2017-06-10)
(S)-carbonyl reductase II (SCRII) from Candida parapsilosis is a short-chain alcohol dehydrogenase/reductase. It catalyses the conversion of 2-hydroxyacetophenone to (S)-1-phenyl-1,2-ethanediol with low efficiency. Sortase was reported as a molecular "stapler" for site-specific protein conjugation to strengthen or add protein functionality.

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