| Company Name: |
Alta Scientific Co., Ltd.
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| Tel: |
022-6537-8550 15522853686 |
| Email: |
sales@altasci.com.cn |
| Products Intro: |
Product Name:Flamprop (free acid)
CAS:58667-63-3
Purity:0.99 Package:10mg, 100mg, 1g
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| Company Name: |
Nanjing Shizhou Biology Technology Co.,Ltd
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| Tel: |
025-025-85560043 17301488900 |
| Email: |
info@synzest.com |
| Products Intro: |
Product Name:2-[N-(3-chloro-4-fluorophenyl)-1-phenylformamido
]propanoic acid
CAS:58667-63-3
Purity:95% Package:1g；5g;10g
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| | FLAMPROP Basic information |
| Product Name: | FLAMPROP | | Synonyms: | FLAMPROP;N-benzoyl-N-(3-chloro-4-fluorophenyl)-DL-alanine;Flamprop acid;Alanine, N-benzoyl-N-(3-chloro-4-fluorophenyl)-;2-[N-(3-chloro-4-fluorophenyl)-1-phenylformamido
]propanoic acid;N-benzoyl-N-(3-chloro-4-fluorophenyl)alanine;C13649000 Flamprop (freEacid);Flamprop 10 μg/ml Acetonitrile | | CAS: | 58667-63-3 | | MF: | C16H13ClFNO3 | | MW: | 321.73 | | EINECS: | | | Product Categories: | | | Mol File: | 58667-63-3.mol |  |
| | FLAMPROP Chemical Properties |
| Boiling point | 516.1±50.0 °C(Predicted) | | density | 1.392±0.06 g/cm3(Predicted) | | pka | 3.53±0.10(Predicted) |
| | FLAMPROP Usage And Synthesis |
| Description | Flamprop is an obsolete herbicide usually formulated as the methyl variant. It has a moderate aqueous solubility and is not volatile. It can be persistent in soil systems. Very little data is available regarding its toxicity to biodiversity but it does appear to be moderately toxic to aquatic species. It has a low oral toxicity to mammals including humans. | | Uses | Flamprop is an antiparasitic agent. A herbicide. | | Definition | ChEBI: Flamprop is a member of benzamides. | | Production Methods | Flamprop is commercially produced through a multi-step synthesis involving the formation of its alanine-based structure. The process begins with the preparation of 3-chloro-4-fluoroaniline, which is acylated with benzoyl chloride to form N-benzoyl-3-chloro-4-fluoroaniline. This intermediate is then coupled with DL-alanine or its derivatives under controlled conditions to yield flamprop. The reaction is typically carried out in organic solvents such as ethyl acetate or toluene, with temperature and pH carefully regulated to optimise yield and purity. | | Mechanism of action | Selective. The mode of action of flamprop is primarily the inhibition of cell elongation at the meristematic regions of the plant. | | Pesticide Type | Herbicide; Metabolite |
| | FLAMPROP Preparation Products And Raw materials |
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