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'''Dimethyl carbate''' is an ].<ref>{{cite web | url = http://www.alanwood.net/pesticides/dimethyl%20carbate.html | title = Dimethyl carbate | publisher = AlanWood.net}}</ref> It can be prepared by the ] of ] and ].<ref>{{cite journal | title = Aluminum chloride catalyzed diene condensation. II. Stronger adherence to the Alder endo rule | author = Inukai, Takashi; Kojima, Takeshi | journal = |
'''Dimethyl carbate''' is an ].<ref>{{cite web | url = http://www.alanwood.net/pesticides/dimethyl%20carbate.html | title = Dimethyl carbate | publisher = AlanWood.net}}</ref> It can be prepared by the ] of ] and ].<ref>{{cite journal | title = Aluminum chloride catalyzed diene condensation. II. Stronger adherence to the Alder endo rule | author = Inukai, Takashi; Kojima, Takeshi | journal = Journal of Organic Chemistry | year = 1966 | volume = 31 | pages = 2032–2033 | issn = 0022-3263 | doi=10.1021/jo01344a543}}</ref> | ||
==References== | ==References== |
Revision as of 02:10, 30 November 2015
Not to be confused with Dimethyl carbonate.Names | |
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IUPAC name Dimethyl (1R,2S,3R,4S)-bicyclohept-5-ene-2,3-dicarboxylate | |
Other names Dimethyl cis-5-norbornene-2,3-dicarboxylate ; Dimalone | |
Identifiers | |
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Properties | |
Chemical formula | C11H14O4 |
Molar mass | 210.229 g·mol |
Density | 1.4852 g/cm |
Melting point | 38 °C (100 °F; 311 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Dimethyl carbate is an insect repellent. It can be prepared by the Diels–Alder reaction of dimethyl maleate and cyclopentadiene.
References
- ^ Merck Index, 11th Edition, 3230
- "Dimethyl carbate". AlanWood.net.
- Inukai, Takashi; Kojima, Takeshi (1966). "Aluminum chloride catalyzed diene condensation. II. Stronger adherence to the Alder endo rule". Journal of Organic Chemistry. 31: 2032–2033. doi:10.1021/jo01344a543. ISSN 0022-3263.
{{cite journal}}
: CS1 maint: multiple names: authors list (link)
External links
- Dimethyl carbate, PAN Pesticides Database
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