C112208
环戊醇
99%
别名:
1-环戊醇, 环戊醇, 羟基环戊烷
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关于此项目
线性分子式:
C5H9OH
化学文摘社编号:
分子量:
86.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-504-8
Beilstein/REAXYS Number:
1900556
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2
InChI key
XCIXKGXIYUWCLL-UHFFFAOYSA-N
SMILES string
OC1CCCC1
assay
99%
form
liquid
Quality Level
refractive index
n20/D 1.453 (lit.)
bp
139-140 °C (lit.)
mp
−19 °C (lit.)
density
0.948 g/mL at 20 °C, 0.949 g/mL at 25 °C (lit.)
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Application
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。
signalword
Warning
hcodes
pcodes
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
123.8 °F - closed cup
flash_point_c
51 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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)
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
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)
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
Synthesis of high density aviation fuel with cyclopentanol derived from lignocellulose.
Sheng X, et al.
Scientific Reports, 5(1), 9565-9565 (2015)
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