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trans-2,3-Butylene carbonate
Skeletal formula of trans-2,3-butylene carbonate
Ball-and-stick model of the trans-2,3-butylene carbonate molecule
Names
IUPAC name
trans-4,5-Dimethyl-[1,3]dioxolan-2-one
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C5H8O3/c1-3-4(2)8-5(6)7-3/h3-4H,1-2H3/t3-,4-/m0/s1 ☒N
    Key: LWLOKSXSAUHTJO-IMJSIDKUSA-N ☒N
  • InChI=1/C5H8O3/c1-3-4(2)8-5(6)7-3/h3-4H,1-2H3/t3-,4-/m0/s1
    Key: LWLOKSXSAUHTJO-IMJSIDKUBM
  • O=C1O[C@@H](C)[C@@H](O1)C
  • O=C1O[C@@H](C)[C@H](C)O1
Properties
C5H8O3
Molar mass 116.116 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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trans-2,3-Butylene carbonate is an organic compound with formula C
5H
8O
3, or (H3C)2(C2H2)(CO3). It is an ester with a carbonate functional group bonded to both free ends of the trans-2,3-butylene group. It is also a heterocyclic compound with a five-membered ring containing two oxygen atoms, and can be viewed as a derivative of dioxolane, namely trans-4,5-dimethyl-1,3-dioxolan-2-one.

The compound is an aprotic polar solvent and has been proposed as an ingredient of the electrolyte of lithium batteries.[1]

See also[edit]

References[edit]

  1. ^ Geun-Chang Chung, Hyeong-Jin Kim, Song-Hui Jun and Myung-Hwan Kim (1999), New cyclic carbonate solvent for lithium ion batteries: trans-2,3-butylene carbonate. Electrochemistry Communications, volume 1, issue 10, pages 493-496. doi:10.1016/S1388-2481(99)00101-0
source: https://en.wikipedia.org/wiki/Trans-2,3-Butylene_carbonate

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