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C112208

Sigma-Aldrich

Cyclopentanol

99%

Sinonimo/i:

1-Cyclopentanol, Cyclopentyl alcohol, Hydroxycyclopentane

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About This Item

Formula condensata:
C5H9OH
Numero CAS:
96-41-3
Peso molecolare:
86.13
Beilstein:
1900556
Numero CE:
202-504-8
Numero MDL:
MFCD00001363
Codice UNSPSC:
12352100
ID PubChem:
24892351
NACRES:
NA.22

Livello qualitativo

100

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.453 (lit.)

P. eboll.

139-140 °C (lit.)

Punto di fusione

−19 °C (lit.)

Densità

0.948 g/mL at 20 °C
0.949 g/mL at 25 °C (lit.)

Stringa SMILE

OC1CCCC1

InChI

1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2
XCIXKGXIYUWCLL-UHFFFAOYSA-N

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Applicazioni

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.

Pittogrammi

Flame
GHS02

Avvertenze

Warning

Indicazioni di pericolo

H226

Consigli di prudenza

P210 - P370 + P378

Classi di pericolo

Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

123.8 °F - closed cup

Punto d’infiammabilità (°C)

51 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK1849
STBK0873
STBJ8014
STBJ7303
STBJ6011

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Three-component coupling reactions of silyl glyoxylates, vinyl Grignard reagent, and nitroalkenes: an efficient, highly diastereoselective approach to nitrocyclopentanols.
Gregory R Boyce et al.
Angewandte Chemie (International ed. in English), 49(47), 8930-8933 (2010-10-16)
Marie Bøjstrup et al.
Organic & biomolecular chemistry, 3(9), 1738-1745 (2005-04-29)
Four aminocyclopentanols, as mimics of putative intermediates in the hydrolysis of alpha-d-galactosides, have been synthesized through a number of stereoselective transformations using the cis-fused cyclopentane-1,4-lactone (1R, 5S, 7R, 8R)-7,8-dihydroxy-2-oxabicyclo[3.3.0]oct-3-one as a chiral building block. The compounds were tested towards various
Gregory R Boyce et al.
Organic letters, 14(2), 652-655 (2012-01-13)
The three-component coupling of Mg acetylides, silyl glyoxylates, and nitroalkenes results in a highly diastereoselective Kuwajima-Reich/vinylogous Michael cascade that provides tetrasubstituted silyloxyallene products. The regio- and diastereoselectivity were studied using DFT calculations. These silyloxyallenes were converted to cyclopentenols and cyclopentitols
E Leroy et al.
Organic letters, 1(5), 775-777 (2000-05-24)
[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
R N Hanson et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 38(8), 641-645 (1987-01-01)
Radioiododestannylations was employed to prepare a series of four specifically labeled thienyl alcohols: 1-(5-iodo-2-thienyl)-cyclopentan-1-ol and -cyclohexan-1-ol; 17 alpha-(5-iodo-2-thienyl)-17 beta-estradiol and -estradiol-3-O-methyl ether. The method utilized 5-(trimethylstannyl)thienyl intermediates which had been prepared in good yields from 2,5-bis(trimethylstannyl)thiophene and the appropriate cyclic
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