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Methyl 3-methyl-4-nitrobenzoate

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Methyl 3-methyl-4-nitrobenzoate Basic information

Product Name:
Methyl 3-methyl-4-nitrobenzoate
Synonyms:
  • Methyl 3-Methyl-4-nitrobenzoate , 98.0%(GC)
  • 4-NITRO-M-TOLUIC ACID METHYL ESTER
  • BENZOIC ACID, 3-METHYL-4-NITRO-METHYL ESTER
  • BUTTPARK 62\04-20
  • METHYL 3-METHYL-4-NITROBENZENECARBOXYLATE
  • METHYL 3-METHYL-4-NITROBENZOATE
  • 3-METHYL-4-NITROBENZOIC ACID METHYL ESTER
  • 3-methyl-4-nitro benzoate
CAS:
24078-21-5
MF:
C9H9NO4
MW:
195.17
EINECS:
230-886-6
Product Categories:
  • FINE Chemical & INTERMEDIATES
  • Benzoic acid
  • Esters
  • Phenyls & Phenyl-Het
  • pharmaceutical intermediates
  • blocks
  • Carboxes
  • NitroCompounds
  • Aromatic Esters
Mol File:
24078-21-5.mol
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Methyl 3-methyl-4-nitrobenzoate Chemical Properties

Melting point:
80 °C
Boiling point:
318.5±30.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Yellow
InChIKey
IEFONJKJLZFGKQ-UHFFFAOYSA-N
CAS DataBase Reference
24078-21-5(CAS DataBase Reference)
NIST Chemistry Reference
M-toluic acid, 4-nitro-, methyl ester(24078-21-5)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22
Safety Statements 
24/25
HS Code 
2916399090

MSDS

  • Language:English Provider:ALFA
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Methyl 3-methyl-4-nitrobenzoate Usage And Synthesis

Chemical Properties

Off-white or light yellow powder

Uses

The presence of the nitro group contributes to its potential reactivity and polar nature, while the methyl ester group enhances its solubility in organic solvents. Methyl 3-methyl-4-nitrobenzoate is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals.

Synthesis

67-56-1

3113-71-1

24078-21-5

Step 1. Synthesis of methyl 3-methyl-4-nitrobenzoate 3-Methyl-4-nitrobenzoic acid (30 g, 165.61 mmol) was dissolved in methanol (300 mL), stirred at 0°C and thionyl chloride (25 mL) was added slowly and dropwise. The reaction mixture was warmed to 80°C and stirring was continued for 1 hour. Upon completion of the reaction, the mixture was concentrated under reduced pressure to give the crude product. The crude product was dissolved in petroleum ether (100 mL) and filtered to give methyl 3-methyl-4-nitrobenzoate as a white solid (31 g, 96% yield). Product Characterization: LC/MS (ES, m/z): [M + H]+ 196.01 1H-NMR (300MHz, CD3Cl) δ 7.99-8.04 (m, 3H), 3.98 (s, 3H), 2.64 (s, 3H)

References

[1] Patent: US2012/277224, 2012, A1. Location in patent: Page/Page column 33
[2] Chemical Communications, 2012, vol. 48, # 94, p. 11558 - 11560
[3] Chemical Communications, 2007, # 5, p. 504 - 506
[4] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 14, p. 4582 - 4589
[5] Chemistry - An Asian Journal, 2010, vol. 5, # 7, p. 1573 - 1585

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