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Merck

254355

Sigma-Aldrich

2-氯丙烯

98%

别名:

2-氯-1-丙烯, 异丙烯基氯

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About This Item

线性分子式:
CH3CCl=CH2
CAS号:
分子量:
76.52
Beilstein:
1361376
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.395 (lit.)

bp

22.5-22.8 °C (lit.)

mp

−138.6 °C (lit.)

密度

0.899 g/mL at 25 °C (lit.)

官能基

alkyl halide
chloro

儲存溫度

2-8°C

SMILES 字串

CC(Cl)=C

InChI

1S/C3H5Cl/c1-3(2)4/h1H2,2H3

InChI 密鑰

PNLQPWWBHXMFCA-UHFFFAOYSA-N

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一般說明

Kinetics of thermal decomposition of 2-chloropropene over 600-1400K temperature range has been investigated. High-quality mass-analyzed threshold ionization spectrum of 2-chloropropene has been reported.

應用

2-Chloropropene has been used in measurement of photoionization cross sections of allyl and 2-propenyl radicals to form C3H5+ by tunable vacuum ultraviolet synchrotron radiation coupled with photofragment translational spectroscopy.

象形圖

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訊號詞

Danger

危險聲明

危險分類

Eye Irrit. 2 - Flam. Liq. 1 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

-4.0 °F - closed cup

閃點(°C)

-20 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Determination of absolute photoionization cross sections for isomers of C3H5: allyl and 2-propenyl radicals.
Robinson JC, et al.
Chemical Physics Letters, 383(5), 601-605 (2004)
Yong Jin Bae et al.
The Journal of chemical physics, 123(4), 044306-044306 (2005-08-13)
A high-quality mass-analyzed threshold ionization (MATI) spectrum of 2-chloropropene, 2-C3H5Cl, is reported. Its ionization energy determined for the first time from the 0-0 band position was 9.5395+/-0.0006 eV. Almost all the peaks in the MATI spectrum could be vibrationally assigned
María E Tucceri et al.
The journal of physical chemistry. A, 117(40), 10218-10227 (2013-09-17)
A detailed theoretical study of the kinetics of the thermal decomposition of 2-chloropropene over the 600-1400 K temperature range has been done. The reaction takes place through the elimination of HCl with the concomitant formation of propyne or allene products.

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