方案
99%
表单
liquid
折射率
n20/D 1.453 (lit.)
沸点
139-140 °C (lit.)
mp
−19 °C (lit.)
密度
0.948 g/mL at 20 °C
0.949 g/mL at 25 °C (lit.)
SMILES字符串
OC1CCCC1
InChI
1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2
InChI key
XCIXKGXIYUWCLL-UHFFFAOYSA-N
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应用
环戊醇可用作：
- 采用Fe3+-蒙脱石催化剂通过Friedel–Crafts烷基化反应制备烷基化芳香族化合物的烷基化试剂。
- 醇与酸酐或酰基氯的酰化反应的反应物。
- 通过Guerbet反应合成高密度多环航空燃料的基质。
警示用语：
Warning
危险声明
预防措施声明
危险分类
Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
123.8 °F - closed cup
闪点(°C)
51 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Fe3+-montmorillonite: A bifunctional catalyst for one pot Friedel-Crafts alkylation of arenes with alcohols.
Choudary BM, et al.
Catalysis Communications, 3(8), 363-367 (2002)
S Dallet et al.
Biochimica et biophysica acta, 1294(1), 15-24 (1996-05-02)
A comparison between the pressure effects on the catalysis of Thermoanaerobium brockii alcohol dehydrogenase (TBADH: a thermostable tetrameric enzyme) and yeast alcohol dehydrogenase (YADH: a mesostable tetrameric enzyme) revealed a different behaviour. YADH activity is continuously inhibited by an increase
May Xiao-Wu Jiang et al.
The Journal of organic chemistry, 70(7), 2824-2827 (2005-03-25)
[reaction: see text] Enzymatic resolution of Boc-protected 4-aminocyclopenten-1-ol 4c gave both enantiomers 5c and 6c in high ee. Boc removal and separate condensation with chloropyrazolopyrimidine 18 provided elaborated 1,4-aminocyclopentenol derivatives 20 and 26, respectively. Separate treatment of 20 and 26
Marie Bøjstrup et al.
Organic & biomolecular chemistry, 5(19), 3164-3171 (2007-09-20)
Bicyclic cyclopentane lactones, prepared from bromodeoxyaldonolactones, were transformed into aminocyclopentanols with an Overman rearrangement as the key step. Two of the compounds prepared, 7 and 19, were found to be good inhibitors of jack bean alpha-mannosidase and beta-D-N-acetylglucosaminidase, respectively.
Highly efficient acylation of alcohols, amines and thiols under solvent-free and catalyst-free conditions.
Ranu BC, et al.
Green Chemistry, 5(1), 44-46 (2003)
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