CAS No: 403-43-0
Product Name: 4-Fluorobenzoyl chloride
Other Name:
4-Fluorobenzoyl chloride
parafluorobenzoyl chloride
para-fluorobenzoic acid chloride
4-(Chloroacetyl)-1-fluorobenzene
p-Fluorobenzoic acid chloride
4-Fluorbenzolcarbonylchlorid
4-fluorobenzoic acid chloride
p-Fluorobenzoyl chloride
4-Fluorobenzoyl chloride
Density: 1.3±0.1 g/cm3
Boiling Point: 180.6±13.0 °C at 760 mmHg
Melting Point: 10-12 °C(lit.)
Molecular Formula: C7H4ClFO
Molecular Weight: 158.557
Flash Point: 82.2±0.0 °C
Exact Mass: 157.993469
PSA: 17.07000
LogP: 2.43
Vapour Pressure: 0.9±0.3 mmHg at 25°C
Index of Refraction: 1.520
Storage condition: 2-8°C
Specification
Appearance: Colorless transparent liquid
Assay: ≥99.0%
Benzoyl chloride: ≤0.1%
Free acid: ≤0.3%
Application
Intermediates of Flumorph CAS: 211867-47-9.
Be used as pesticide intermediate, mainly used in the synthesis of the fungicide Flumorph.
4-Fluorobenzoyl Chloride is used in the synthesis of tryphostins which act as inhibitors of EGF receptor and Erb82/neu tyrosine kinases. Also used in the synthesis of 1,2,4-triazole-3-thiones as antidepressant agents.
Package: 25kg/drum, can also be designed according to customer requirements.
Storage: Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.Repackaging capabilities to fit customer specific requirements.Synthesis of reference compounds, intermediates, drug candidates, impurities and metabolites for customers with a range of milligrams to kilograms (including GMP quality).By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.
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