268941
cis-2-Heptene
97%
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About This Item
Formula condensata:
CH3(CH2)3CH=CHCH3
Numero CAS:
Peso molecolare:
98.19
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
Prodotti consigliati
![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)
Tensione di vapore
87 mmHg ( 37.7 °C)
Saggio
97%
Stato
liquid
Indice di rifrazione
n20/D 1.407 (lit.)
P. ebollizione
98-99 °C (lit.)
Densità
0.708 g/mL at 25 °C (lit.)
Stringa SMILE
[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-
OTTZHAVKAVGASB-HYXAFXHYSA-N
Descrizione generale
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].
Applicazioni
cis-2-Heptene (alkene) was used in the synthesis of the corresponding bis(10-phenoxathiiniumyl)alkane adduct[2].
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
21.2 °F - closed cup
Punto d’infiammabilità (°C)
-6 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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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