C19651
Chloroacetonitrile
99%
동의어(들):
α-Chloroacetonitrile, 2-Chloroacetonitrile, Chloromethyl cyanide, Cyanomethyl chloride, Monochloroacetonitrile
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모든 사진(3)
About This Item
Linear Formula:
ClCH2CN
CAS Number:
Molecular Weight:
75.50
Beilstein:
506028
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
3 (vs air)
vapor pressure
1.78 psi ( 20 °C)
분석
99%
양식
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
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애플리케이션
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.
신호어
Danger
유해 및 위험 성명서
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 Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
129.2 °F
Flash Point (°C)
54 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
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)
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)
The photoredox-catalyzed Meerwein addition reaction: intermolecular amino-arylation of alkenes.
Prasad Hari D, et al.
Angewandte Chemie (International Edition in English), 53(3), 725-728 (2014)
Total synthesis of (-)-apicularen A.
Su Q and Panek JS
Journal of the American Chemical Society, 126(8), 2425-2430 (2004)
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