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About This Item
Linear Formula:
CH3(CH2)3CH=CHCH3
CAS Number:
Molecular Weight:
98.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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![1-METHYL-4-[1-(4-METHYLPHENYL)VINYL]BENZENE AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/413/183/71bb24e3-bc94-4dd1-9f74-63583773a435/640/71bb24e3-bc94-4dd1-9f74-63583773a435.png)
vapor pressure
87 mmHg ( 37.7 °C)
Assay
97%
form
liquid
refractive index
n20/D 1.407 (lit.)
bp
98-99 °C (lit.)
density
0.708 g/mL at 25 °C (lit.)
SMILES string
[H]\C(C)=C(/[H])CCCC
InChI
1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3-
InChI key
OTTZHAVKAVGASB-HYXAFXHYSA-N
General description
The rate constants for the epoxidation of cis-2-heptene with meta-chloroperbenzoic acid (mCPBA) and [2-percarboxyethyl]-functionalized silica in different solvents were studied[1].
Application
cis-2-Heptene (alkene) was used in the synthesis of the corresponding bis(10-phenoxathiiniumyl)alkane adduct[2].
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
21.2 °F - closed cup
Flash Point(C)
-6 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Rossella Mello et al.
Organic & biomolecular chemistry, 12(20), 3246-3250 (2014-04-15)
The rate constants for the epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica (1a) and meta-chloroperbenzoic acid (mCPBA) (1b) in different solvents have been determined at temperatures in the -10 to 40 °C range. The heterogeneous epoxidation exhibits a dependence of the
Bing-Jun Zhao et al.
The Journal of organic chemistry, 72(16), 6154-6161 (2007-07-03)
Addition of phenoxathiin cation radical (PO*+) to acyclic alkenes in acetonitrile (MeCN) solution occurred stereospecifically to form bis(10-phenoxathiiniumyl)alkane adducts. Stereospecific trans addition is ascribed to the intermediacy of an episulfonium cation radical. The alkenes used were cis- and trans-2-butene, cis-
Hiroyuki Ohno et al.
Journal of AOAC International, 97(5), 1452-1458 (2015-04-24)
A headspace GC/MS method was developed for identification and quantitation of residual volatile organic compounds in poly(methyl methacrylate) (PMMA) kitchen utensils. A sample was cut into small pieces, then N,N-dimethylacetamide was added in a headspace vial and sealed. After storing
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