| Company Name: |
Shanghai Jiegu Biotechnology Co., Ltd.
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| Tel: |
021-51698675 |
| Email: |
sales@jiejiegroup.com |
| Products Intro: |
Product Name:3-Thiophenecarboxylic acid, 4-[[[(4,5-dihydro-3-methoxy-4-methyl-5-oxo-1H-1,2,4-triazol-1-yl)carbonyl]amino]sulfonyl]-5-methyl-
CAS:936331-72-5
Purity:97% HPLC Package:100KG;1KG
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| Company Name: |
TLC Pharmaceutical Standards Ltd.
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| Tel: |
18012923235 18012923235 |
| Email: |
chinasales04@tlcstandards.com.cn |
| Products Intro: |
Product Name:Thiencarbazone (Thiencarbazone-Methyl Metabolite M01)
CAS:936331-72-5
Purity:95%+ HPLC；Assay：467%+ Package:10mg;25mg;50mg;100mg
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| | 3-Thiophenecarboxylic acid, 4-[[[(4,5-dihydro-3-methoxy-4-methyl-5-oxo-1H-1,2,4-triazol-1-yl)carbonyl]amino]sulfonyl]-5-methyl- Basic information |
| | 3-Thiophenecarboxylic acid, 4-[[[(4,5-dihydro-3-methoxy-4-methyl-5-oxo-1H-1,2,4-triazol-1-yl)carbonyl]amino]sulfonyl]-5-methyl- Chemical Properties |
| | 3-Thiophenecarboxylic acid, 4-[[[(4,5-dihydro-3-methoxy-4-methyl-5-oxo-1H-1,2,4-triazol-1-yl)carbonyl]amino]sulfonyl]-5-methyl- Usage And Synthesis |
| Uses | Thiencarbazone is a herbicide, as well as metabolite of relevant pesticides. | | Definition | ChEBI: Thiencarbazone is an N-sulfonylurea in which the sulfur atom is attached to a 4-carboxy-2-methylthiophen-3-yl group and in which the non-sulfonated nitrogen is substituted by a 3-methoxy-4-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl group. It is a metabolite of the herbicide, thiencarbazone-methyl. It has a role as a herbicide, an agrochemical, an EC 2.2.1.6 (acetolactate synthase) inhibitor and a metabolite. It is a thiophenecarboxylic acid, a N-sulfonylurea, an ether and a member of triazoles. | | Production Methods | Industrial manufacture of thiencarbazone is normally as the methyl variant and generally follows a streamlined heterocycle-building sequence typical of modern sulfonylaminocarbonyl herbicides. Production begins with preparation of the key thiophene-based precursor, usually via acylation and cyclisation steps that introduce the substituted thiophene core. In parallel, the carbazone fragment is assembled through controlled reaction of a sulfonyl isocyanate or related activated carbonyl species with an appropriate amine, forming the sulfonylaminocarbonyl linkage that defines the class. These two fragments are then coupled under dehydrating or activating conditions to form the final heterocyclic urea-like structure. | | Mechanism of action | ALS inhibitor, systemic, absorbed by roots and leaves, contact and residual action | | Pesticide Type | Herbicide |
| | 3-Thiophenecarboxylic acid, 4-[[[(4,5-dihydro-3-methoxy-4-methyl-5-oxo-1H-1,2,4-triazol-1-yl)carbonyl]amino]sulfonyl]-5-methyl- Preparation Products And Raw materials |
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