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C105805

Sigma-Aldrich

Cyclohexanemethanol

ReagentPlus®, ≥99%

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Synonym(s):
(Hydroxymethyl)cyclohexane, Cyclohexyl methanol, Hexahydrobenzyl alcohol, NSC 5288
Linear Formula:
C6H11CH2OH
CAS Number:
Molecular Weight:
114.19
Beilstein:
773712
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

product line

ReagentPlus®

Assay

≥99%

form

liquid

refractive index

n20/D 1.465 (lit.)

bp

181 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

SMILES string

OCC1CCCCC1

InChI

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

InChI key

VSSAZBXXNIABDN-UHFFFAOYSA-N

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This Item
PHR28981154605C105104
Cyclohexanemethanol ReagentPlus®, ≥99%

Sigma-Aldrich

C105805

Cyclohexanemethanol

Cyclohexylmethanol pharmaceutical secondary standard, certified reference material

Supelco

PHR2898

Cyclohexylmethanol

Cyclohexylmethanol United States Pharmacopeia (USP) Reference Standard

USP

1154605

Cyclohexylmethanol

2-Cyclohexylethanol 99%

Sigma-Aldrich

C105104

2-Cyclohexylethanol

form

liquid

form

-

form

-

form

liquid

refractive index

n20/D 1.465 (lit.)

refractive index

n20/D 1.465 (lit.)

refractive index

n20/D 1.465 (lit.)

refractive index

n20/D 1.465 (lit.)

bp

181 °C (lit.)

bp

181 °C (lit.)

bp

181 °C (lit.)

bp

206-207 °C/745 mmHg (lit.)

density

0.928 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

product line

ReagentPlus®

product line

-

product line

-

product line

-

Application

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.

Legal Information

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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25G
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705578-5MG-PW

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MMYOMAG-74K-13

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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.
Mohamed OS, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 200(2-3), 209-215 (2008)

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