| Company Name: |
Shanghai Jiegu Biotechnology Co., Ltd.
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| Tel: |
021-51698675 |
| Email: |
sales@jiejiegroup.com |
| Products Intro: |
Product Name:Triaziflam [iso]
CAS:131475-57-5
Purity:97% HPLC Package:100KG;1KG
|
| Company Name: |
Hubei Guangao Biotechnology Co., Ltd
|
| Tel: |
027-02702759223056 18162699093 |
| Email: |
1208480011@qq.com |
| Products Intro: |
CAS:131475-57-5
Purity:99% HPLC Package:25KG;200KG;5KG;1KG;1T
|
| Company Name: |
Hubei Wande Chemical Co., Ltd
|
| Tel: |
15377098680 15377098680 |
| Email: |
1148280011@qq.com |
| Products Intro: |
CAS:131475-57-5
Purity:99% HPLC Package:25KG;200KG;5KG;1KG;1T
|
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| | Triaziflam [iso] Basic information |
| Product Name: | Triaziflam [iso] | | Synonyms: | Triaziflam [iso];(RS)-N-[2-(3,5-Dimethylphenoxy)-1-methylethyl]-6-(1-fluoro-1-methylethyl)-1,3,5-triazine-2,4-diamine;Triaziflam@100 μg/mL in Methanol;Triaziflam Standard;1,3,5-Triazine-2,4-diamine, N2-[2-(3,5-dimethylphenoxy)-1-methylethyl]-6-(1-fluoro-1-methylethyl)-;Triaziflam | | CAS: | 131475-57-5 | | MF: | C17H24FN5O | | MW: | 333.4 | | EINECS: | | | Product Categories: | | | Mol File: | 131475-57-5.mol | ![Triaziflam [iso] Structure](CAS/20180808/GIF/131475-57-5.gif) |
| | Triaziflam [iso] Chemical Properties |
| Melting point | 100～105℃ | | Boiling point | 540.0±60.0 °C(Predicted) | | density | 1.187±0.06 g/cm3(Predicted) | | pka | 4.01±0.10(Predicted) | | BRN | 13916125 |
| Risk Statements | 52 | | WGK Germany | 3 |
| | Triaziflam [iso] Usage And Synthesis |
| Definition | ChEBI: N-[1-(3,5-dimethylphenoxy)propan-2-yl]-6-(2-fluoropropan-2-yl)-1,3,5-triazine-2,4-diamine is a diamino-1,3,5-triazine that is 1,3,5-triazine substituted by a [1-(3,5-dimethylphenoxy)propan-2-yl]nitrilo group, amino group and 2-fluoropropan-2-yl group at positions 2,4 and 6, respectively. It is a diamino-1,3,5-triazine, an organofluorine compound, a secondary amino compound and an aromatic ether. | | Production Methods | The industrial production of triaziflam involves constructing a 1,3,5-triazine ring substituted with two amino groups. One position is functionalised with a 2-fluoropropan-2-yl group, while another is linked to a [1-(3,5-dimethylphenoxy)propan-2-yl] moiety via nucleophilic substitution. This yields the active compound, triaziflam. | | Mechanism of action | Triaziflam inhibits of the photosystem II electron transport and cellulose biosynthesis.Long lasting action and non-selective. Acts at multiple sites on the weed. | | Pesticide Type | Herbicide |
| | Triaziflam [iso] Preparation Products And Raw materials |
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