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Merck
CN

196169

3-Methylcyclopentanol, mixture of isomers

99%

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About This Item

Linear Formula:
CH3C5H8OH
CAS Number:
Molecular Weight:
100.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
242-540-1
MDL number:
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Product Name

3-Methylcyclopentanol, mixture of isomers, 99%

InChI key

VEALHWXMCIRWGC-UHFFFAOYSA-N

InChI

1S/C6H12O/c1-5-2-3-6(7)4-5/h5-7H,2-4H2,1H3

SMILES string

CC1CCC(O)C1

assay

99%

form

liquid

refractive index

n20/D 1.446 (lit.)

bp

149-150 °C (lit.)

density

0.91 g/mL at 25 °C (lit.)

functional group

hydroxyl

Application

3-Methylcyclopentanol has been used in the synthesis of pentacycloalkoxy-substituted phosphazenes and 3-methyl cyclopentylbromide.

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

131.0 °F - closed cup

flash_point_c

55 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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A Synthetic Procedure for Secondary Bromides from Alcohols.
Jenkins GL and Kellett Jr JC.
The Journal of Organic Chemistry, 27(2), 624-625 (1962)
The synthesis and characterization of cycloalkoxy-linear phosphazenes.
Ozturk AI, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 178(10), 2097-2105 (2003)
Mireia Oromí-Farrús et al.
Journal of analytical methods in chemistry, 2012, 452949-452949 (2012-06-01)
The use of iodine as a catalyst and either acetic or trifluoroacetic acid as a derivatizing reagent for determining the enantiomeric composition of acyclic and cyclic aliphatic chiral alcohols was investigated. Optimal conditions were selected according to the molar ratio

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