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| UNII_Ref = {{fdacite|correct|FDA}} | | UNII_Ref = {{fdacite|correct|FDA}} | ||
| UNII = BN2PH0TQOD | | UNII = BN2PH0TQOD | ||
| PubChem = | | PubChem = 10921747 | ||
| ChEBI = 136029 | |||
| ChemSpiderID = 10430159 | | ChemSpiderID = 10430159 | ||
| SMILES = O=C(OC)2(C(=O)OC)\1C2/C=C/1 | | SMILES = O=C(OC)2(C(=O)OC)\1C2/C=C/1 |
Revision as of 02:45, 12 November 2018
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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3D model (JSmol) | |
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CompTox Dashboard (EPA) | |
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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) |
Pharmacology | |
ATC code | P03BX05 (WHO) |
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.
External links
- Dimethyl carbate, PAN Pesticides Database
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