추천 제품
형태
liquid
농도
70 wt. % in toluene
refractive index
n20/D 1.456
density
0.963 g/mL at 25 °C
작용기
alkyl halide
chloro
저장 온도
2-8°C
SMILES string
ClCC#C
InChI
1S/C3H3Cl/c1-2-3-4/h1H,3H2
InChI key
LJZPPWWHKPGCHS-UHFFFAOYSA-N
일반 설명
Product is the 70wt.% solution of propargyl chloride in toluene. Propargyl chloride is a propargyl halide. Its trimethylsilylation reaction has been reported. Liquid-phase Raman spectra, and vapor-phase and solution-phase infrared spectra of propargyl chloride has been studied at 100-3400cm-1 and 300-3800cm-1, respectively. It participates in the addition reaction with acyclic 1,3-dienes (at -78°C) in the presence of zinc chloride.
애플리케이션
Propargyl chloride may be used as propargylating agent in the preparation of arabinogalactan propargyl ethers with degree of substitution up to 1.8. It may be used for the in situ preparation of propargyltrichlorosilane and allenyltrichlorosilane, required for the synthesis of optically active allenic and homopropargylic alcohols.
Propargyl chloride solution may be used for the enantioselective synthesis of enantiomerically enriched homopropargyl alcohols.
신호어
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Repr. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3
표적 기관
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
66.2 °F
Flash Point (°C)
19 °C
The vibrational spectra and vibrational assignments of the propargyl halides.
Spectrochimica Acta Part A: Molecular Spectroscopy, 19(7), 1153-1163 (1963)
Zinc chloride catalyzed addition reactions of propargyl chlorides with acyclic 1, 3-dienes.
The Journal of Organic Chemistry, 46(20), 4097-4100 (1981)
Chemo-and enantioselective catalytic addition of propargyl chloride to aldehydes promoted by [Cr (Salen)] complexes.
Tetrahedron Asymmetry, 12(7), 1063-1069 (2001)
Selective synthesis of optically active allenic and homopropargylic alcohols from propargyl chloride.
Tetrahedron Asymmetry, 12(22), 2449-2452 (2002)
Trimethylsilylation of Propargyl Chloride and Propargyl Bromide.
Synthetic Communications, 20(21), 3375-3378 (1990)
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