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Benthiavalicarb

Benthiavalicarb Suppliers list
Company Name: Shanghai Changyan Chem & Tech Co., Ltd.  
Tel: 021-20242659 18930833303
Email: sales@changyanchem.cn
Company Name: Shenzhen Newcore Chemical Technology Co., Ltd.  
Tel: 13612807752
Email: ncchemical@163.com
Company Name: Shanghai Jiegu Biotechnology Co., Ltd.  
Tel: 021-51698675
Email: sales@jiejiegroup.com
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
Benthiavalicarb Basic information
Product Name:Benthiavalicarb
Synonyms:Benthiavalicarb;Benthiavalicarb [iso];Carbamic acid, N-[(1S)-1-[[[(1R)-1-(6-fluoro-2-benzothiazolyl)ethyl]amino]carbonyl]-2-methylpropyl]-;Benthiavalicarb (free acid);[(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid
CAS:413615-35-7
MF:C15H18FN3O3S
MW:339.39
EINECS:
Product Categories:
Mol File:413615-35-7.mol
Benthiavalicarb Structure
Benthiavalicarb Chemical Properties
LogP2.270 (est)
Safety Information
MSDS Information
Benthiavalicarb Usage And Synthesis
DescriptionBenthiavalicarb is a fungicide that is usually used as the isopropyl variant. It is not highly toxic to mammals or fauna and flora.
DefinitionChEBI: 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 MethodsBenthiavalicarb 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.
OriginBenthiavalicarb has been developed by Kumiai Chemicals Industry for treatment of tomatoes and potato late blight.
Mechanism of actionProtective and curative action with residual effects, inhibits phospholipid biosynthesis
Pesticide TypeFungicide
Benthiavalicarb Preparation Products And Raw materials
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