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4-Bromo-3-nitrobenzoic acid

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CAS:6319-40-0
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4-Bromo-3-nitrobenzoic acid manufacturers

  • 4-Bromo-3-nitrobenzoic acid
  • 4-Bromo-3-nitrobenzoic acid pictures
  • $100.00 / 1KG
  • 2023-12-26
  • CAS:6319-40-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
4-Bromo-3-nitrobenzoic acid Basic information
Product Name:4-Bromo-3-nitrobenzoic acid
Synonyms:RARECHEM AH CK 0042;4-BROMO-3-NITROBENZOIC ACID;4-BROMO-3-NITRO-BENZOIC ACID >97%;3-Nitro-4-bromobenzoic acid;2-Bromo-5-carboxynitrobenzene;4-Bromo-3-nitrobenzoic Acid >;Benzoic acid, 4-bromo-3-nitro-;4-Bromo-3-nitrobenzoicaci
CAS:6319-40-0
MF:C7H4BrNO4
MW:246.01
EINECS:
Product Categories:intermediate;Benzoic acid;blocks;Bromides;Carboxes;NitroCompounds;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:6319-40-0.mol
4-Bromo-3-nitrobenzoic acid Structure
4-Bromo-3-nitrobenzoic acid Chemical Properties
Melting point 202-204°C
Boiling point 340.9±32.0 °C(Predicted)
density 2.0176 (rough estimate)
refractive index 1.6200 (estimate)
storage temp. 2-8°C
solubility soluble in Methanol
form Solid
pka3.35±0.10(Predicted)
color White to yellow
CAS DataBase Reference6319-40-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39
WGK Germany 3
Hazard Note Irritant
HS Code 29163990
MSDS Information
4-Bromo-3-nitrobenzoic acid Usage And Synthesis
Chemical Propertieslight yellow powder
Synthesis
4-Bromobenzoic acid

586-76-5

4-Bromo-3-nitrobenzoic acid

6319-40-0

The general procedure for the synthesis of 4-bromo-3-nitrobenzoic acid from 4-bromobenzoic acid is as follows: 1. prepare a nitration mixture by slowly adding fuming nitric acid (12.4 mL, 0.3 mol) to concentrated hydrochloric acid followed by sulfuric acid (30.1 mL, 0.6 mol) at 0-5 °C. 2. the cooled nitrification mixture was transferred to a beaker fitted with a mechanical stirrer and a charging funnel. 3. 4-Bromobenzoic acid (40 g, 0.2 mol) was slowly added to the nitrification mixture in batches while maintaining a temperature of 0-5°C. The dosing process lasted for 5 hours. 4. After completion of the addition, the reaction mixture was continued to be stirred at room temperature for 2 hours. 5. The reaction mixture was slowly poured into ice water to precipitate the solid product. 6. The solid product was separated by filtration, washed with water to neutrality and subsequently air dried to constant weight to give the pure 4-bromo-3-nitrobenzoic acid (white solid, 47.2 g, 96% yield). Product characterization data: 1H NMR (300 MHz, CDCl3): δ 7.85 (d, J = 12.0 Hz, 1H), 8.09 (d, J = 12.0 Hz, 1H), 8.48 (s, 1H). 13C NMR (75 MHz, CDCl3): δ 124.2, 132.1, 135.2, 138.0, 139.8, 159.8, 171.0.

References[1] Beilstein Journal of Organic Chemistry, 2016, vol. 12, p. 2267 - 2273
[2] Patent: US2008/293736, 2008, A1. Location in patent: Page/Page column 32
[3] Patent: WO2017/7634, 2017, A1. Location in patent: Paragraph 0730; 0731; 0732
[4] Patent: WO2005/16882, 2005, A1. Location in patent: Page/Page column 13
[5] Justus Liebigs Annalen der Chemie, 1884, vol. 222, p. 178 Anm. 1
4-Bromo-3-nitrobenzoic acid Preparation Products And Raw materials
Raw materials4-Bromo-3-nitrotoluene-->4-Bromobenzoic acid
Preparation Products3-Bromo-4-(trifluoromethyl)benzoic acid-->3-Amino-4-bromobenzoic acid-->Methyl 3-amino-4-bromobenzoate
Tag:4-Bromo-3-nitrobenzoic acid(6319-40-0) Related Product Information
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