Benthiavalicarb
- CAS No.
- 413615-35-7
- Chemical Name:
- Benthiavalicarb
- Synonyms
- Benthiavalicarb;Benthiavalicarb [iso];Benthiavalicarb (free acid);[(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid;Carbamic acid, N-[(1S)-1-[[[(1R)-1-(6-fluoro-2-benzothiazolyl)ethyl]amino]carbonyl]-2-methylpropyl]-
- CBNumber:
- CB91120098
- Molecular Formula:
- C15H18FN3O3S
- Molecular Weight:
- 339.39
- MDL Number:
- MFCD33395039
- MOL File:
- 413615-35-7.mol
| LogP | 2.270 (est) |
|---|---|
| FDA UNII | 6YZ3ZXJ6WN |
Benthiavalicarb price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Biosynth | FF102474 | [(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid | 413615-35-7 | 1mg | $900 | 2026-06-04 | Buy |
| Biosynth | FF102474 | [(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid | 413615-35-7 | 2mg | $900 | 2026-06-04 | Buy |
| Biosynth | FF102474 | [(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid | 413615-35-7 | 5mg | $1298 | 2026-06-04 | Buy |
| Biosynth | FF102474 | [(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid | 413615-35-7 | 10mg | $2076.8 | 2026-06-04 | Buy |
| Biosynth | FF102474 | [(2S)-1-{[(1R)-1-(6-Fluoro-1,3-Benzothiazol-2-Yl)Ethyl]Amino}-3-Methyl-1-Oxo-2-Butanyl]Carbamic Acid | 413615-35-7 | 25mg | $4867.5 | 2026-06-04 | Buy |
Benthiavalicarb Chemical Properties, Uses, Production
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
Benthiavalicarb Preparation Products And Raw materials
Raw materials
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Shanghai Changyan Chem & Tech Co., Ltd. | 021-20242659 18930833303 | sales@changyanchem.cn | China | 4998 | 55 |
| Shenzhen Newcore Chemical Technology Co., Ltd. | 13612807752 | ncchemical@163.com | China | 289 | 55 |
| Shanghai Jiegu Biotechnology Co., Ltd. | 021-51698675 | sales@jiejiegroup.com | China | 8198 | 58 |
| Energy Chemical | 021-58432009 400-005-6266 | marketing@energy-chemical.com | China | 44871 | 58 |
