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Dimethyl carbate: Difference between revisions

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==References== ==References==
{{Reflist}} {{Reflist}}

==External links==


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Revision as of 04:20, 10 December 2021

Not to be confused with Passion pro carbonate.
Dimethyl carbate
Names
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
  • InChI=1S/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+Key: VGQLNJWOULYVFV-SPJNRGJMSA-N
  • InChI=1/C11H428h34/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+Key: VGQLNJWOULYVFV-SPJNRGJMBT
SMILES
  • O=C(OC)2(C(=O)OC)\1C2/C=C/1
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
Chemical compound

Dimethyl carbate is an insect repellent. It can be prepared by the Diels–Alder reaction of dimethyl maleate and cyclopentadiene.

References

  1. ^ Merck Index, 11th Edition, 3230
  2. 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.


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