196169
3-Methylcyclopentanol, mixture of isomers
99%
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About This Item
Linear Formula:
CH3C5H8OH
CAS Number:
Molecular Weight:
100.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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
SMILES string
CC1CCC(O)C1
InChI
1S/C6H12O/c1-5-2-3-6(7)4-5/h5-7H,2-4H2,1H3
InChI key
VEALHWXMCIRWGC-UHFFFAOYSA-N
Application
3-Methylcyclopentanol has been used in the synthesis of pentacycloalkoxy-substituted phosphazenes and 3-methyl cyclopentylbromide.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
131.0 °F - closed cup
Flash Point(C)
55 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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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
A Synthetic Procedure for Secondary Bromides from Alcohols.
Jenkins GL and Kellett Jr JC.
The Journal of Organic Chemistry, 27(2), 624-625 (1962)
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