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线性分子式:
CH3C5H8OH
化学文摘社编号:
分子量:
100.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
242-540-1
MDL number:
Assay:
99%
Form:
liquid
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.
A Synthetic Procedure for Secondary Bromides from Alcohols.
Jenkins GL and Kellett Jr JC.
The Journal of Organic Chemistry, 27(2), 624-625 (1962)
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
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)
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