| Identification | Back Directory | [Name]
5-chloro-7-bromo-8-quinolyl vinyl carbonate | [CAS]
34462-96-9 | [Synonyms]
CGA-30599
Acriquinate
5-chloro-7-bromo-8-quinolyl vinyl carbonate
Acrylic acid 7-bromo-5-chloroquinolin-8-yl ester
2-Propenoic acid, 7-bromo-5-chloro-8-quinolinyl ester | [EINECS(EC#)]
252-049-4 | [Molecular Formula]
C12H7BrClNO2 | [MDL Number]
MFCD01696304 | [MOL File]
34462-96-9.mol | [Molecular Weight]
312.55 |
| Hazard Information | Back Directory | [Definition]
ChEBI: Halacrinate is a member of quinolines. | [Production Methods]
Halacrinate is synthesised through a multi-step chemical process beginning with the construction of a quinoline ring, typically via a Skraup or Doebner–Miller reaction using aniline derivatives and carbonyl compounds. The quinoline core is then selectively halogenated to introduce chlorine at position 5 and bromine at position 7 through electrophilic aromatic substitution. Next, the 8-position is activated, often by hydroxylation, to enable esterification. The final step involves coupling the activated quinoline with acrylic acid or acryloyl chloride to form the prop-2-enoate ester, completing the Halacrinate molecule. | [Mechanism of action]
Protective and curative. Quinoline fungicides work by inhibiting dihydroorotate dehydrogenase (DHODH), an enzyme crucial for pyrimidine biosynthesis in fungal cells. | [Pesticide Type]
Fungicide |
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