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Merck
CN

481378

SAFC

烯丙基氯

别名:

3-氯-1-丙烯, 氯丙烯

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线性分子式:
CH2=CHCH2Cl
化学文摘社编号:
分子量:
76.52
Beilstein:
635704
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.21
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蒸汽密度

2.6 (vs air)

质量水平

蒸汽压

20.58 psi ( 55 °C)
5.71 psi ( 20 °C)

方案

98.0% (returnable containers)

expl. lim.

11.2 %

折射率

n20/D 1.414 (lit.)

沸点

44-46 °C (lit.)

mp

−130 °C (lit.)

密度

0.939 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

ClCC=C

InChI

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

InChI key

OSDWBNJEKMUWAV-UHFFFAOYSA-N

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警示用语:

Danger

危险分类

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

靶器官

Nervous system,Liver,Kidney, Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

-25.6 °F

闪点(°C)

-32 °C

个人防护装备

Eyeshields, Faceshields, Gloves

法规信息

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历史批次信息供参考:

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Lot/Batch Number

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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)
Justin M Chalker et al.
Chemical communications (Cambridge, England), (25)(25), 3714-3716 (2009-06-27)
Multiple, complementary methods are reported for the chemical conversion of cysteine to S-allyl cysteine on protein surfaces, a useful transformation for the exploration of olefin metathesis on proteins.
Heike Burghart-Stoll et al.
Organic letters, 13(10), 2730-2733 (2011-04-30)
A (DHQN)(2)AQN-promoted asymmetric dihydroxylation (92% ee) of the allyl chloride derived from enynol (E)-13 and an 8-step sequence provided access to the hydroxyethylated furanone (R)-21. Oxidation with MnO(2) furnished 50% furanone (+)-(R)-2a and 2.7% isomeric furanone (+)-(R)-3a. (R)-2a possesses the
Kai Abersfelder et al.
Journal of the American Chemical Society, 130(12), 4114-4121 (2008-03-04)
The rearrangements of (chlorosilyl)disilenes R2(Cl)Si-(Tip)Si=SiTip2 (5a,b: Tip = 2,4,6-iPr3C6H2, a: R = Me, b: R = Ph) quantitatively yield the isomeric chlorocyclotrisilanes (6a,b). The disilene precursors 5a,b are, in turn, accessible from the reactions of the disilenide Tip2Si=Si(Tip)Li (1), that
Richard M Lopachin et al.
Toxicological sciences : an official journal of the Society of Toxicology, 95(1), 136-146 (2006-10-07)
Acrylamide (ACR) is a conjugated type-2 alkene that produces synaptic toxicity presumably by sulfhydryl adduction. The alpha,beta-unsaturated carbonyl of ACR is a soft electrophile and, therefore, adduction of nucleophilic thiol groups could occur through a conjugate (Michael) addition reaction. To

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