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Key Documents

236306

Sigma-Aldrich

烯丙基氯

ReagentPlus®, 99%

同義詞:

3-氯-1-丙烯, 氯丙烯

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About This Item

線性公式:
CH2=CHCH2Cl
CAS號碼:
分子量::
76.52
Beilstein:
635704
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

2.6 (vs air)

品質等級

蒸汽壓力

20.58 psi ( 55 °C)
5.71 psi ( 20 °C)

產品線

ReagentPlus®

化驗

99%

形狀

liquid

expl. lim.

11.2 %

折射率

n20/D 1.414 (lit.)

bp

44-46 °C (lit.)

mp

−130 °C (lit.)

溶解度

alcohol: miscible(lit.)
chloroform: miscible(lit.)
diethyl ether: miscible(lit.)
petroleum ether: miscible(lit.)
water: slightly soluble(lit.)

密度

0.939 g/mL at 25 °C (lit.)

官能基

alkyl halide
chloro

儲存溫度

2-8°C

SMILES 字串

ClCC=C

InChI

1S/C3H5Cl/c1-2-3-4/h2H,1,3H2

InChI 密鑰

OSDWBNJEKMUWAV-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

氯丙烯与过氧化氢环氧化的动力学过程已有报道

應用

氯丙烯:
  • 已用作 193 nm 激光闪光光解产生烯丙基自由基的前体
  • 已用于 α,ω-双官能团化学中间体的合成(通过 交叉复分解反应)

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

標靶器官

Nervous system,Liver,Kidney, Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

-25.6 °F

閃點(°C)

-32 °C

個人防護裝備

Eyeshields, Faceshields, Gloves


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Cross-metathesis reactions of allyl chloride with fatty acid methyl esters: Efficient synthesis of a, ?-difunctional chemical intermediates from renewable raw materials.
Jacobs T, et al.
Applied Catalysis A: General, 353(1), 32-35 (2009)
Lars Seidel et al.
Molecules (Basel, Switzerland), 18(11), 13608-13622 (2013-11-07)
Photochemically driven reactions involving unsaturated radicals produce a thick global layer of organic haze on Titan, Saturn's largest moon. The allyl radical self-reaction is an example for this type of chemistry and was examined at room temperature from an experimental
Epoxidation of allyl chloride with hydrogen peroxide catalyzed by titanium silicalite 1.
Gao H, et al.
Applied Catalysis A: General, 138(1), 27-38 (1996)
Carbocycle synthesis through facile and efficient palladium-catalyzed allylative de-aromatization of naphthalene and phenanthrene allyl chlorides.
Shirong Lu et al.
Angewandte Chemie (International ed. in English), 47(23), 4366-4369 (2008-04-30)
Vikas Sikervar et al.
The Journal of organic chemistry, 77(11), 5132-5138 (2012-04-27)
A coupling strategy for the synthesis of 2,4-dimethyl-1α,25(OH)(2)D(3) is achieved which involves methylation of a pro-A ring vinyl sulfone and in situ traping of the allyl sulfonyl anion with a CD ring allyl chloride. TBAF-promoted 1,2-eliminative desulfonylation and concomitant silyl

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