Isoprothiolane

Chemical Information
Isoprothiolane is a malonate ester that is diisopropyl malonate in which the two methylene hydrogens at position 2 are replaced by a 1,3-dithiolan-2-ylidene group. An insecticide and fungicide used to control a range of diseases including Pyricularia oryzae, Helminthosporium sigmoideum and Fusarium nivale. It has a role as an insecticide, an environmental contaminant, a phospholipid biosynthesis inhibitor and an antifungal agrochemical. It is an isopropyl ester, a malonate ester and a member of dithiolanes. It is functionally related to a malonic acid. It derives from a hydride of a 1,3-dithiolane.
| CAS Number | 50512-35-1 |
| PubChem CID | 39681 |
| IUPAC Name | dipropan-2-yl 2-(1,3-dithiolan-2-ylidene)propanedioate |
| Molecular Formula | C12H18O4S2 |
| Molecular Weight | 290.4 |
| XLogP | 3.3 |
| Topological Polar Surface Area | 103 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 329 |
| Property | Value |
|---|---|
| Molecular Weight | 290.4 |
| XLogP3 | 3.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 290.06465140 |
| Monoisotopic Mass | 290.06465140 |
| Topological Polar Surface Area | 103 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 329 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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