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C105805

Sigma-Aldrich

Cyclohexanemethanol

ReagentPlus®, ≥99%

Sinonimo/i:

(Hydroxymethyl)cyclohexane, Cyclohexyl methanol, Hexahydrobenzyl alcohol, NSC 5288

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About This Item

Formula condensata:
C6H11CH2OH
Numero CAS:
100-49-2
Peso molecolare:
114.19
Beilstein:
773712
Numero CE:
202-857-8
Numero MDL:
MFCD00001510
Codice UNSPSC:
12352100
ID PubChem:
24891964
NACRES:
NA.22

Nome Commerciale

ReagentPlus®

Saggio

≥99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.465 (lit.)

P. eboll.

181 °C (lit.)

Densità

0.928 g/mL at 25 °C (lit.)

Stringa SMILE

OCC1CCCCC1

InChI

1S/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2
VSSAZBXXNIABDN-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

Cyclohexanemethanol (Cyclohexyl methanol) can be used as a starting material for the synthesis of cyclohexanecarboxaldehyde, cyclohexanecarboxylic acid, cyclohexanone, and 1,4-cyclohexadione by photocatalytic oxidation (PCO) using titanium dioxide nanoparticles as a catalyst.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

170.6 °F - closed cup

Punto d’infiammabilità (°C)

77 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificati d'analisi (COA)

Lot/Batch Number
WXBD5452V
WXBD3865V
WXBD2775V
WXBD1070V
WXBC8330V

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Yasunori Okada et al.
Organic letters, 9(8), 1573-1576 (2007-03-16)
[reaction: see text] Ethyl 1-thio-2,3,4,6-tetrakis-O-triisopropylsilyl-beta-d-glucopyranoside, ethyl 6-O-benzyl-1-thio-2,3,4-tris-O-triisopropylsilyl-beta-d-glucopyranoside, and ethyl 6-O-pivaloyl-1-thio-2,3,4-tris-O-triisopropylsilyl-beta-d-glucopyranoside induced highly beta-selective O-glucosidations. Among them, the 6-O-pivaloylated substrate provided the best selectivity up to alpha/beta = 3:97 with cyclohexylmethanol, and the substrate was used for glucosidations with secondary and
Rabea Schlüter et al.
Applied microbiology and biotechnology, 103(10), 4137-4151 (2019-04-04)
The cycloalkanes, comprising up to 45% of the hydrocarbon fraction, occur in crude oil or refined oil products (e.g., gasoline) mainly as alkylated cyclohexane derivatives and have been increasingly found in environmental samples of soil and water. Furthermore, short-chain alkylated
Nanoparticles TiO2-photocatalyzed oxidation of selected cyclohexyl alcohols.
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