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About This Item
Linear Formula:
C5H7CH3
CAS Number:
Molecular Weight:
82.14
Beilstein/REAXYS Number:
1900640
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
form
liquid
bp
72 °C/754 mmHg (lit.)
density
0.78 g/mL at 25 °C (lit.)
SMILES string
CC1=CCCC1
InChI
1S/C6H10/c1-6-4-2-3-5-6/h4H,2-3,5H2,1H3
InChI key
ATQUFXWBVZUTKO-UHFFFAOYSA-N
Application
1-Methylcyclopentene can be used as:
- A probe molecule in the synthesis of alkenyl carbenium ions via adsorption on zeolite Y.
- A model olefin compound in the kinetic study of hydrogenation of olefins using various catalytic systems.
- A reactant to synthesize 1,2,3-trisubstituted benzocyclopentenes by reacting with β-disulfonyl iodonium ylides.
accessory
Product No.
Description
Pricing
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
-2.2 °F - closed cup
flash_point_c
-19 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Certificates of Analysis (COA)
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Customers Also Viewed
Formation of stable alkenyl carbenium ions in high yield by adsorption of 1-methylcyclopentene on zeolite Y at low temperature
Yang S, et al.
Chemical Communications (Cambridge, England), 2008-2009 (2001)
Kinetic study of olefin hydrogenation on hydrotreating catalysts
Badawi M, et al.
J. Mol. Catal. A: Chem., 320, 34-39 (2010)
A facile diastereoselective synthesis of functionalized 1, 2, 3-trisubstituted benzocyclopentenes through the cycloaddition of bis (phenylsulfonyl) iodonium ylides to cyclic alkenes
Adam W, et al.
The Journal of Organic Chemistry, 68, 9155-9158 (2003)
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