| Identification | Back Directory | [Name]
Benthiavalicarb | [CAS]
413615-35-7 | [Synonyms]
Benthiavalicarb
Benthiavalicarb [iso]
Carbamic acid, N-[(1S)-1-[[[(1R)-1-(6-fluoro-2-benzothiazolyl)ethyl]amino]carbonyl]-2-methylpropyl]- | [Molecular Formula]
C15H18FN3O3S | [MDL Number]
MFCD33395039 | [MOL File]
413615-35-7.mol | [Molecular Weight]
339.39 |
| Hazard Information | Back Directory | [Description]
Benthiavalicarb is a fungicide that is usually used as the isopropyl variant. It is not highly toxic to mammals or fauna and flora. | [Definition]
ChEBI: A carboxamide resulting from the formal condensation of the carboxy group of L-valine with (1R)-1-(6-fluoro-1,3-benzothiazol-2-yl)ethylamine and replacement of one of the hydrogens attached to the alpha-am
no group by a carboxy group. It is the active form of the fungicide benthiavalicarb isopropyl (in which the carbamic acid group has been converted to the corresponding isopropyl ester). | [Production Methods]
Benthiavalicarb is commercially synthesised through a multi-step process that constructs its valinamide carbamate fungicidal structure. The synthesis begins with the preparation of a fluorinated benzothiazole intermediate, which is then coupled with a valine-derived amine to form a urea linkage. This intermediate is further reacted with isopropyl chloroformate to introduce the isopropyl ester group, yielding benthiavalicarb-isopropyl. The process requires precise control of stereochemistry, as the compound exists as a mixture of R-L and S-L isomers. | [Origin]
Benthiavalicarb has been developed by Kumiai Chemicals Industry for treatment of tomatoes and potato late blight.
| [Mechanism of action]
Protective and curative action with residual effects, inhibits phospholipid biosynthesis | [Pesticide Type]
Fungicide |
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| Company Name: |
Energy Chemical
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| Telephone: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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