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| IUPACName = Dimethyl (1''R'',2''S'',3''R'',4''S'')-bicyclohept-5-ene-2,3-dicarboxylate | | IUPACName = Dimethyl (1''R'',2''S'',3''R'',4''S'')-bicyclohept-5-ene-2,3-dicarboxylate | ||
| OtherNames = Dimethyl ''cis''-5-norbornene-2,3-dicarboxylate |
| OtherNames = Dimethyl ''cis''-5-norbornene-2,3-dicarboxylate; Dimalone | ||
|Section1={{Chembox Identifiers | |Section1={{Chembox Identifiers | ||
| CASNo = 39589-98-5 | | CASNo = 39589-98-5 |
Revision as of 03:56, 24 February 2019
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) | |
ChEBI | |
ChemSpider | |
PubChem CID | |
UNII | |
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) |
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
- 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
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