Key Documents

View All Documentation

C112208

Cyclopentanol

Name: Cyclopentanol
Brand: ALDRICH

99%

Synonym(s):

1-Cyclopentanol, Cyclopentyl alcohol, Hydroxycyclopentane

Select a Size

Change View

About This Item

Linear Formula:

C₅H₉OH

CAS Number:

96-41-3

Molecular Weight:

86.13

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892351

EC Number:

202-504-8

Beilstein/REAXYS Number:

1900556

MDL number:

MFCD00001363

Assay:

99%

Form:

liquid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

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

Description

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.
A reactant in the acylation of alcohols with an acid anhydride or acid chloride.
A substrate in the synthesis of high-density polycyclic aviation fuel by the Guerbet reaction.

Still not finding the right product?

Explore all of our products under Cyclopentanol

pictograms

GHS02

signalword

Warning

hcodes

H226

pcodes

P210 - P370 + P378

Hazard Classifications

Flam. Liq. 3

Storage Class

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

Regulatory Information

危险化学品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Cloning and characterization of a gene cluster involved in cyclopentanol metabolism in Comamonas sp. strain NCIMB 9872 and biotransformations effected by Escherichia coli-expressed cyclopentanone 1,2-monooxygenase.

Hiroaki Iwaki et al.

Applied and environmental microbiology, 68(11), 5671-5684 (2002-10-31)

Cyclopentanone 1,2-monooxygenase, a flavoprotein produced by Pseudomonas sp. strain NCIMB 9872 upon induction by cyclopentanol or cyclopentanone (M. Griffin and P. W. Trudgill, Biochem. J. 129:595-603, 1972), has been utilized as a biocatalyst in Baeyer-Villiger oxidations. To further explore this

Diastereoselective multicomponent cyclizations of Fischer carbene complexes, lithium enolates, and allylmagnesium bromide leading to highly substituted five- and six-membered carbocycles.

José Barluenga et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 12(27), 7225-7235 (2006-08-24)

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

Total synthesis of (-)-norzoanthamine.

Daisuke Yamashita et al.

Angewandte Chemie (International ed. in English), 48(8), 1404-1406 (2008-12-05)

No bones about it: (-)-Norzoanthamine, a promising candidate for an anti-osteoporotic drug, was the target of a total synthesis (see scheme). The final bisaminal formation with AcOH/H(2)O gave the DEFG ring, while the cyclization precursor was prepared by installing the

View All Related Papers

Global Trade Item Number

SKU	GTIN
C112208-100ML	04061833460825
C112208-500ML	04061833460849
C112208-5ML	04061837637599