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| Section1 = {{Chembox Identifiers | | Section1 = {{Chembox Identifiers | ||
| CASNo = 39589-98-5 | | CASNo = 39589-98-5 | ||
| |
| CASNo_Ref = {{cascite|correct|}} | ||
| PubChem = | | PubChem = | ||
| ChemSpiderID = 10430159 | | ChemSpiderID = 10430159 | ||
| ATCCode_prefix = P03 | |||
| ATCCode_suffix = BX05 | |||
| SMILES = O=C(OC)2(C(=O)OC)\1C2/C=C/1 | | SMILES = O=C(OC)2(C(=O)OC)\1C2/C=C/1 | ||
| InChI = 1/C11H14O4/c1-14-10(12)8-6-3-4-7(5-6)9(8)11(13)15-2/h3-4,6-9H,5H2,1-2H3/t6-,7+,8-,9+ | | InChI = 1/C11H14O4/c1-14-10(12)8-6-3-4-7(5-6)9(8)11(13)15-2/h3-4,6-9H,5H2,1-2H3/t6-,7+,8-,9+ | ||
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{{antiinfective-drug-stub}} |
Revision as of 16:57, 3 February 2013
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 | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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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. ISSN 6.
{{cite journal}}
: Check|issn=
value (help)CS1 maint: multiple names: authors list (link)
External links
- Dimethyl carbate, PAN Pesticides Database
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