4-Fluoro-3-nitrobenzoic acid

4-Fluoro-3-nitrobenzoic acid
  • CAS No.:453-71-4

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
4-Fluoro-3-nitrobenzoic acid Chemical Properties
Melting point 123-126 °C (lit.)
Boiling point 92°C 15mm
density 1.5071 (estimate)
Fp 92°C/15mm
storage temp. Sealed in dry,Room Temperature
solubility 95% ethanol: soluble50mg/mL, clear, light yellow
pka3.54±0.10(Predicted)
form Powder or Crystals
color Light yellow to tan
Water Solubility insoluble
BRN 2107562
CAS DataBase Reference453-71-4(CAS DataBase Reference)
NIST Chemistry Reference4-Fluoro-3-nitrobenzoic acid(453-71-4)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36-24/25
WGK Germany 2
HazardClass IRRITANT
HS Code 29163990
MSDS Information
ProviderLanguage
4-Fluoro-3-nitrobenzoic acid English
ACROS English
SigmaAldrich English
ALFA English
4-Fluoro-3-nitrobenzoic acid Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses4-Fluoro-3-nitrobenzoic acid was used:
  • as starting reagent in the preparation of novel benzimidazoles having antimycobacterial activity
  • in preparation of series of novel acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors containing benzimidazole core structure
  • in preparation of bis(heterocyclic) skeletal precursors for the Pictet-Spengler reaction
  • in solid-phase synthesis of trisubstituted [1,3,5]triazino[1,2-a]benzimidazole-2,4(3H,10H)-diones

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