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107-14-2 - Chloroacetonitrile, 98+% - A12825 - Alfa Aesar

A12825 Chloroacetonitrile, 98+%

Codice CAS
107-14-2
Sinonimi

Dimensioni Prezzo ($) Quantità Disponibilità
100g 21,20
500g 79,60
1kg 127,00
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Chloroacetonitrile, 98+%

MDL
MFCD00001885
EINECS
203-467-0

Proprietà chimiche

Formula
C2H2ClN
Peso formula
75.50
Punto di ebollizione
124-126°
Punto di infiammabilità
56°(132°F)
Densità
1.195
Indice di rifrazione
1.4230
Solubilità
Immiscible with water.

Applicazioni

Chloroacetonitrile is used in the electrochemical synthesis of cyanoacetic acid with carbon dioxide. It is involved in phase-transfer-catalyzed Darzen's condensation reaction with cyclohexanone. It is also used as an eluent additive in thermospray liquid chromatography/mass spectrometry. Further, it is used to prepare polysubstituted pyrido[1,2-a]benzimidazole by reacting with other reactant such as malononitrile, aromatic aldehyde and pyridine.

Note

Incompatible with strong oxidizing agents and acids.

Letteratura

Forms cyanomethyl esters with carboxylic acids, e.g. in the presence of Et3N, which are a useful protection method; the esters are readily cleaved by Na2S in aqueous acetone: Synth. Commun., 22, 693 (1992).

Good yields of ß-hydroxy nitriles have been obtained by Reformatsky-type reaction with aldehydes and ketones using Zn and TMS chloride: Tetrahedron Lett., 31, 2205 (1990). See Bromoacetonitrile, A13933.

In the presence of base, Darzens condensation with aldehydes and ketones, under conventional or phase-transfer conditions, gives glycidonitriles (cyano epoxides), readily converted to the homologated carboxylic acids, esters or aldehydes with loss of cyanide: J. Chem. Soc., Chem. Commun., 988 (1974); Coll. Czech. Chem. Commun., 53, 822 (1988).

Ritter reaction with tertiary alcohols yields 2-chloroacetamides which, on treatment with thiourea, provides a high-yield conversion of tertiary alcohols to the corresponding amines: Synthesis, 1709 (2000):

For use in vicarious nucleophilic substitution of hydrogen in nitro-substituted hetereocycles, see 2-Nitrothiophene, A17464.

Hoseini, S. J.; Nasrabadi, H.; Fath, R. H.; Moradi, Z.; Rashidi, M. Oxidative Addition of Propargyl Halides, Chloroacetonitrile, and Ethyl Chloroacetate to a Dimethylplatinum(II) Complex: Kinetic and DFT Studies. Organometallics 2014, 33 (7), 1689-1699.

Kimura, S. Y.; Komaki, Y.; Plewa, M. J.; Marinas, B. J. Chloroacetonitrile and N,2-Dichloroacetamide Formation from the Reaction of Chloroacetaldehyde and Monochloramine in Water. Environ. Sci. Technol. 2013, 47 (21), 12382-12390.

Rischio GHS e dichiarazioni precauzionali

Dichiarazioni di rischio (UE): H226-H301-H310-H331

Flammable liquid and vapour. Toxic if swallowed. Fatal in contact with skin. Toxic if inhaled.

Dichiarazioni precauzionali: P210-P261-P301+P310a-P303+P361+P353-P405-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Avoid breathing dust/fume/gas/mist/vapours/spray. IF SWALLOWED: IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Altri riferimenti

Beilstein
506028
Classe di rischio
6.1
Gruppo di imballaggio
I
Codice tariffe armonizzato
2926.90
TSCA
Yes
RTECS
AL8225000

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