Saflufenacil Inters
114776-15-7
Off-white powder
Water content ≤1%
Purity ≥99.0%
Availability: | |
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Product Description
We are a agrochem intermediates manufacturer of 114776-15-7 2-Chloro-4-fluoro-5-nitrobenzoic Acid.
Its CAS No. is 114776-15-7.
Our agrochem Intermediates can be used in a variety of APIs such as saflufenacil inters,thiencarbazonemethyl inters,pyroxsulam inters,flubendiamide inters,etc.
Product Category | Saflufenacil Inters |
CAS NO | 114776-15-7 |
Product Specifications | Off-white powder Water content ≤1% Purity ≥99.0% |
114776-15-7 2-Chloro-4-fluoro-5-nitrobenzoic Acid.pdf
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114776-15-7 2-Chloro-4-fluoro-5-nitrobenzoic Acid is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .
China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.
yes , you can have 1 114776-15-7 2-Chloro-4-fluoro-5-nitrobenzoic Acid sample for starting the business , but it is not free
please contact sale team for detail.
This compound is mainly used in:
Synthesis of pharmaceuticals: As an intermediate in the production of active pharmaceutical ingredients (APIs).
Organic synthesis: Used in the preparation of various chemicals or as a building block for more complex molecules.
Research applications: Employed in scientific studies to investigate reaction mechanisms or chemical properties.
Like many organic compounds, this compound should be handled with care. Here are a few precautions:
Avoid inhalation or ingestion: Use proper PPE (Personal Protective Equipment) such as gloves and goggles.
Ventilation: Work in a well-ventilated area, preferably a fume hood, to avoid inhaling any vapors.
Storage: Store in a cool, dry place away from heat or sources of ignition. Ensure it is kept in tightly sealed containers.
Toxicity: As with many nitrobenzoic acids, there could be some toxicological risks, especially if ingested, inhaled, or if there is prolonged skin contact.
Environmental impact: Release into the environment should be avoided. It may cause harm to aquatic life.
It can be synthesized by various methods, typically starting from benzoic acid derivatives and introducing the chlorine, fluorine, and nitro groups through electrophilic aromatic substitution reactions or similar synthetic pathways. The specific synthetic route often depends on the desired yield and purity.