2-(2-Chlorophenyl)acetonitrile
2-(2-Chlorophenyl)acetonitrile Basic information
- Product Name:
- 2-(2-Chlorophenyl)acetonitrile
- Synonyms:
-
- 2-Chlorobenzeneacetonitrile
- Acetonitrile, (o-chlorophenyl)-
- Benzeneacetonitrile, 2-chloro-
- OCCN
- O-CHLOROBENZYL CYANIDE
- (O-CHLOROPHENYL)ACETONITRILE
- 2-CHLOROBENZYL CYANIDE
- 2-CHLOROPHENYLACETONITRILE
- CAS:
- 2856-63-5
- MF:
- C8H6ClN
- MW:
- 151.59
- EINECS:
- 220-669-4
- Product Categories:
-
- Aromatic Nitriles
- Mol File:
- 2856-63-5.mol
2-(2-Chlorophenyl)acetonitrile Chemical Properties
- Melting point:
- 24 °C (lit.)
- Boiling point:
- 240-242 °C (lit.)
- Density
- 1
- refractive index
- 1.5425-1.5445
- Flash point:
- >110°C
- storage temp.
- Sealed in dry,Room Temperature
- Water Solubility
- Insoluble in water
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- powder to lump to clear liquid
- color
- White or Colorless to Light yellow
- FreezingPoint
- 22.0 to 25.0 ℃
- BRN
- 2043683
- Exposure limits
- NIOSH: IDLH 25 mg/m3
- CAS DataBase Reference
- 2856-63-5(CAS DataBase Reference)
- NIST Chemistry Reference
- 2-Chlorobenzyl cyanide(2856-63-5)
Safety Information
- Hazard Codes
- T,Xi
- Risk Statements
- 36/37/38-23/24/25
- Safety Statements
- 45-36/37/39-28B-26-22
- RIDADR
- 3276
- WGK Germany
- 3
- Hazard Note
- Irritant
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29269095
MSDS
- Language:English Provider:2-Cyanobenzyl chloride
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2-(2-Chlorophenyl)acetonitrile Usage And Synthesis
Chemical Properties
CLEAR SLIGHTLY YELLOW LIQUID AFTER MELTING
Uses
2-Chlorobenzyl cyanide was used in the synthesis of clopidogrel, platelet aggregation inhibitor.
Synthesis
1058649-12-9
10442-39-4
2856-63-5
GENERAL METHODS: A mixture of MOM-ether (1 mmol) and tetrabutylammonium cyanide (2 mmol) was added to [Hmim][NO3] (0.4 mmol) and the reaction was carried out under microwave irradiation (the reaction temperature was maintained at 135 °C and the power at 170 W). The reaction process was monitored by thin-layer chromatography (TLC) and the eluent was hexane/ethyl acetate (5:1). After completion of the reaction, the mixture was extracted with ether (3 × 10 mL). The organic phases were combined and dried with anhydrous Na2SO4, followed by rotary evaporation to remove the solvent to give the crude product. The crude product was purified by neutral alumina column chromatography with hexane/ethyl acetate (5:1, 75 mL) as the eluent to give high purity o-chlorophenylacetonitrile, the spectral data of which were in agreement with those reported in the literature.
References
[1] Tetrahedron Letters, 2010, vol. 51, # 25, p. 3274 - 3276
[2] Tetrahedron Letters, 2014, vol. 55, # 32, p. 4424 - 4426
2-(2-Chlorophenyl)acetonitrile Preparation Products And Raw materials
Raw materials
Preparation Products
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2-(2-Chlorophenyl)acetonitrile(2856-63-5)Related Product Information
- Calcium chloride
- Mepiquat chloride
- Acetonitrile
- Choline chloride
- 2-Chlorobenzoic acid
- Benzyl chloride
- Ammonium chloride
- Polyvinyl chloride
- 2-Chlorobenzaldehyde
- Sodium chloride
- 2-Chlorophenylacetic acid
- 2-Chlorophenol
- 2,4-Dichlorophenylacetonitrile
- 2-CHLORO-6-FLUOROPHENYLACETONITRILE
- Glycolonitrile
- 2-(4-Amino-2-chloro-5-methylphenyl)-2-(4-chlorophenyl)acetonitrile
- 2,6-Dichlorobenzyl acetonitrile
- 2-Chlorophenyl cyclopentyl ketone