Structure via PubChem · Public domain (PubChem)
bromopropylate
Sign in to saveAlso known as acarol, phenisobromolate, isopropyl bis(4‑bromophenyl)(hydroxy)acetate, isopropyl 4,4′‑dibromobenzilate, isopropyl 4,4'‑dibromobenzilate
Bromopropylate is a chemical compound used as an acaricide against spider mites in apiaries and on fruit crops such as citrus and grapes. It was banned by the European Union in 2011.
In the Vinony graph
Vinony's link graph records 2 inbound references to bromopropylate, and connects out to mass density, chemical formula and melting point.
It is catalogued under topics including 4-Bromophenyl compounds, Acaricides and Carboxylate esters.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C17H16Br2O3
- Molecular weight
- 428.1 g/mol
- IUPAC name
- propan-2-yl 2,2-bis(4-bromophenyl)-2-hydroxyacetate
- SMILES
- CC(C)OC(=O)C(C1=CC=C(C=C1)Br)(C2=CC=C(C=C2)Br)O
- InChIKey
- FOANIXZHAMJWOI-UHFFFAOYSA-N
- XLogP
- 4.8
- Polar surface area
- 46.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 425.946618572
Show 3 more facts
- chemical formula
- C₁₇H₁₆Br₂O₃
- canonical SMILES
- CC(C)OC(=O)C(C1=CC=C(C=C1)Br)(C2=CC=C(C=C2)Br)O
- Commons category
- Bromopropylate
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Preparation
- Gallery
- References
Bromopropylate is a chemical compound used as an acaricide against spider mites in apiaries and on fruit crops such as citrus and grapes. It was banned by the European Union in 2011.
==Preparation== Bromopropylate is prepared by the esterification of the 4,4'-dibromo derivative of benzilic acid with isopropanol. 400px
Excerpted from Wikipedia’s “bromopropylate” article, available under the CC BY-SA 4.0 licence.