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Merck
CN

459798

Sigma-Aldrich

烯丙醇

≥98.5%

别名:

2-丙烯-1-醇

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About This Item

线性分子式:
CH2=CHCH2OH
CAS号:
分子量:
58.08
Beilstein:
605307
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.21

蒸汽密度

2 (vs air)

质量水平

蒸汽压

23.8 mmHg ( 25 °C)

方案

≥98.5%

自燃温度

712 °F

expl. lim.

18 %

折射率

n20/D 1.412 (lit.)

沸点

96-98 °C (lit.)

mp

−129 °C (lit.)

密度

0.854 g/mL at 25 °C (lit.)

官能团

hydroxyl

SMILES字符串

OCC=C

InChI

1S/C3H6O/c1-2-3-4/h2,4H,1,3H2

InChI key

XXROGKLTLUQVRX-UHFFFAOYSA-N

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应用

用于诱导肝脏损坏的小鼠模型,该模型用于研究肝细胞毒性和肝干细胞介导修复的机制。

警示用语:

Danger

危险分类

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

71.6 °F - closed cup

闪点(°C)

22 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Gregory M Mullen et al.
Journal of the American Chemical Society, 136(17), 6489-6498 (2014-04-08)
Partial oxidation of alcohols is a topic of great interest in the field of gold catalysis. In this work, we provide evidence that the partial oxidation of allyl alcohol to its corresponding aldehyde, acrolein, over oxygen-precovered gold surfaces occurs via
Deoxydehydration of glycerol to allyl alcohol catalyzed by rhenium derivatives.
Canale V, et al.
Catalysis Science & Technology, 4(10), 3697-3704 (2014)
Hydrosilylation of allyl alcohol with [HSiMe2OSiO1.5]8: octa (3-hydroxypropyldimethylsiloxy) octasilsesquioxane and its octamethacrylate derivative as potential precursors to hybrid nanocomposites.
Zhang C and Laine RM.
Journal of the American Chemical Society, 122(29), 6979-6988 (2000)
Copper-catalyzed tandem trifluoromethylation/semipinacol rearrangement of allylic alcohols.
Zhi-Min Chen et al.
Angewandte Chemie (International ed. in English), 52(37), 9781-9785 (2013-07-23)
Madeleine C Warner et al.
Organic letters, 14(19), 5094-5097 (2012-09-26)
A general and efficient route for the synthesis of enantiomerically pure α-substituted ketones and the corresponding lactones has been developed. Ruthenium- and enzyme-catalyzed dynamic kinetic resolution (DKR) with a subsequent Cu-catalyzed α-allylic substitution are the key steps of the route.

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