C112208
Cyclopentanol
99%
Synonym(s):
1-Cyclopentanol, Cyclopentyl alcohol, Hydroxycyclopentane
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About This Item
Linear Formula:
C5H9OH
CAS Number:
Molecular Weight:
86.13
Beilstein:
1900556
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
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.)
SMILES string
OC1CCCC1
InChI
1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2
InChI key
XCIXKGXIYUWCLL-UHFFFAOYSA-N
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Related Categories
Application
Cyclopentanol can be used as:
- An alkylating agent in the preparation of alkylated aromatic compounds using Fe3+-montmorillonite catalyst via Friedel–Crafts alkylation reaction.[1]
- A reactant in the acylation of alcohols with an acid anhydride or acid chloride.[2]
- A substrate in the synthesis of high-density polycyclic aviation fuel by the Guerbet reaction.[3]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
123.8 °F - closed cup
Flash Point(C)
51 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The one-pot sequential reaction of a chromium alkoxycarbene complex, a ketone or ester lithium enolate, and allylmagnesium bromide enabled the selective synthesis of novel diastereomerically pure pentasubstituted cyclopentanols or tetrasubstituted 1,4-cyclohexanediols, depending on the degree of substitution at the Cbeta
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[reaction: see text] (1S,2S,3S,4R,5R)-4-amino-5-(hydroxymethyl)cyclopentane-1,2,3-triol 1 is prepared stereoselectively from D-lyxose and displays anomer-selective inhibition for beta-galactosidase (Ki = 3.0 x 10(-6) M) and beta-glucosidase (Ki = 1.5 x 10(-7) M), over alpha-galactosidase (Ki = 2.3 x 10(-5) M) and alpha-glucosidase
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