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Merck

C105805

Sigma-Aldrich

Cyclohexanemethanol

ReagentPlus®, ≥99%

Sinónimos:

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

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About This Item

Fórmula lineal:
C6H11CH2OH
Número de CAS:
Peso molecular:
114.19
Beilstein/REAXYS Number:
773712
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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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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1 of 4

Este artículo
CLS4444500CLS44441LCLS44444L
material

Delong , borosilicate glass

material

Delong , borosilicate glass

material

Delong , borosilicate glass

material

Delong , borosilicate glass

manufacturer/tradename

Corning 4444-125

manufacturer/tradename

Corning 4444-500

manufacturer/tradename

Corning 4444-1L

manufacturer/tradename

Corning 4444-4L

feature

cap: no, closure type Closure cap

feature

cap: no, closure type Closure cap

feature

cap: no, closure type Closure cap

feature

cap: no, closure type Closure cap

packaging

case of 6

packaging

case of 6

packaging

case of 6

packaging

case of 1

flask capacity

125 mL

flask capacity

500 mL

flask capacity

1000 mL

flask capacity

4,000 mL

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.[1]

Legal Information

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

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


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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)
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

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