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4-METHYL-2-NITROBENZOIC ACID

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CAS:27329-27-7
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CAS:27329-27-7
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4-METHYL-2-NITROBENZOIC ACID manufacturers

  • 4-METHYL-2-NITROBENZOIC ACID
  • 4-METHYL-2-NITROBENZOIC ACID pictures
  • $101.00 / 1KG
  • 2025-09-25
  • CAS:27329-27-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
4-METHYL-2-NITROBENZOIC ACID Basic information
Product Name:4-METHYL-2-NITROBENZOIC ACID
Synonyms:4-METHYL-2-NITROBENZOIC ACID 97;2-Nitro-p-toluic acid;NSC 80180;4-Methyl-2-nitrobenzoic acid 97%;Benzoic acid, 4-methyl-2-nitro-;4-METHYL-2-NITROBENZOIC ACID 97 ISO 9001:2015 REACH;4-METHYL-2-NITROBENZOIC ACID
CAS:27329-27-7
MF:C8H7NO4
MW:181.15
EINECS:
Product Categories:C8;Carbonyl Compounds;Carboxylic Acids
Mol File:27329-27-7.mol
4-METHYL-2-NITROBENZOIC ACID Structure
4-METHYL-2-NITROBENZOIC ACID Chemical Properties
Melting point 160-164 °C (lit.)
Boiling point 367.6±30.0 °C(Predicted)
density 1.392±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder
pka2.36±0.25(Predicted)
color Brown
InChI1S/C8H7NO4/c1-5-2-3-6(8(10)11)7(4-5)9(12)13/h2-4H,1H3,(H,10,11)
InChIKeyKZLLSSGOPIGKDO-UHFFFAOYSA-N
SMILESCc1ccc(C(O)=O)c(c1)[N+]([O-])=O
Safety Information
Hazard Codes Xn
Risk Statements 22-43
Safety Statements 37/39
WGK Germany 3
HS Code 2916399090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Skin Sens. 1
MSDS Information
4-METHYL-2-NITROBENZOIC ACID Usage And Synthesis
Uses4-Methyl-2-nitrobenzoic acid is a chemical that can be used for wastewater treatment.
Synthesis
2,5-Dimethylnitrobenzene

89-58-7

4-METHYL-2-NITROBENZOIC ACID

27329-27-7

General procedure for the synthesis of 4-methyl-2-nitrobenzoic acid from 2,5-dimethylnitrobenzene: 1,4-dimethyl-2-nitrobenzene (907 mg, 6 mmol, 1.0 eq.) and sodium hydroxide (1.8 g, 45.0 mmol, 7.5 eq.) were added to a 100 mL autoclave with 10 mL of 80% (v/v) aqueous ethanol (8 mL of ethanol mixed with 2 mL of water). After oxygenation three times, oxygen was passed to a pressure of 1.8 MPa. The reaction was carried out in an oil bath at a controlled temperature of 65 °C for 24 h. After the reaction was completed, the reaction was diluted with methanol. After completion of the reaction, the reaction mixture was diluted with methanol and the pH was adjusted to 2-3. The solvent was removed by distillation under reduced pressure. Ethyl acetate was added for extraction and the organic phase was dried and filtered. The product was separated by column chromatography and 129 mg (0.85 mmol) of unreacted 1,4-dimethyl-2-nitrobenzene was recovered, giving 86% conversion of 1,4-dimethyl-2-nitrobenzene. The target product 4-methyl-2-nitrobenzoic acid 811 mg (4.48 mmol) was obtained in 75% yield.

References[1] Patent: CN106995374, 2017, A. Location in patent: Paragraph 0031; 0032; 0033; 0034; 0035; 0036; 0037-0042
[2] Journal of Organic Chemistry, 2018, vol. 83, # 15, p. 8092 - 8103
Tag:4-METHYL-2-NITROBENZOIC ACID(27329-27-7) Related Product Information
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