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About This Item
Linear Formula:
ClCH2CN
CAS Number:
Molecular Weight:
75.50
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-467-0
Beilstein/REAXYS Number:
506028
MDL number:
Assay:
99%
Form:
liquid
vapor density
3 (vs air)
Quality Level
vapor pressure
1.78 psi ( 20 °C)
assay
99%
form
liquid
refractive index
n20/D 1.422 (lit.)
bp
124-126 °C (lit.)
density
1.193 g/mL at 25 °C (lit.)
SMILES string
ClCC#N
InChI
1S/C2H2ClN/c3-1-2-4/h1H2
InChI key
RENMDAKOXSCIGH-UHFFFAOYSA-N
Application
Chloroacetonitrile can be used:
- For the synthesis of ionic liquids containing nitrile functionalized imidazolium salts.
- For the synthesis of cyanomethyl dodecyl trithiocarbonate, a reversible addition-fragmentation chain transfer (RAFT) agent.
- As an alkylating reagent for the synthesis of derivatives of triazolyl thiazoles to be used as anti-tuberculosis agents.
- As a reagent in photo Meerwein addition reaction for amino-arylation of alkenes.
- As an esterifying agent in the synthesis of a cytotoxic natural product: apicularen A.
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signalword
Danger
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
129.2 °F
flash_point_c
54 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Thiocarbonylthio end group removal from RAFT-synthesized polymers by radical-induced reduction.
Chong YK, et al.
Macromolecules, 40(13), 4446-4455 (2007)
Synthesis and characterization of ionic liquids incorporating the nitrile functionality.
Zhao D, et al.
Inorganic Chemistry, 43(6), 2197-2205 (2004)
Synthesis of new S-derivatives of clubbed triazolyl thiazole as anti-Mycobacterium tuberculosis agents.
Shiradkar MR, et al.
Bioorganic & Medicinal Chemistry, 15(12), 3997-4008 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C19651-100G | 04061833474853 |
| C19651-5G | 04061833474877 |
| C19651-500G | 04061833474860 |


