Basic information Safety Supplier Related

METHYL 4-IODO-3-NITROBENZOATE

Basic information Safety Supplier Related

METHYL 4-IODO-3-NITROBENZOATE Basic information

Product Name:
METHYL 4-IODO-3-NITROBENZOATE
Synonyms:
  • METHYL 4-IODO-3-NITROBENZOATE
  • Methyl-4-iodo-3-nitrobenzoate SynonyMs 4-Iodo-3-Nitrobenzoic Acid Methyl Ester
  • 4-iodo-3-nitrobenzoic acid methyl ester
  • Benzoic acid, 4-iodo-3-nitro-, methyl ester
CAS:
89976-27-2
MF:
C8H6INO4
MW:
307.04
Mol File:
89976-27-2.mol
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METHYL 4-IODO-3-NITROBENZOATE Chemical Properties

Melting point:
103-105°C
Boiling point:
360.1±32.0 °C(Predicted)
Density 
1.904±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
Appearance
Yellow to brown Solid
Water Solubility 
Soluble in DCM 10mg/0.5mL. Insoluble in water.
Sensitive 
Light Sensitive
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Safety Information

Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-37/39
HS Code 
2916399090

MSDS

  • Language:English Provider:ALFA
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METHYL 4-IODO-3-NITROBENZOATE Usage And Synthesis

Uses

Methyl 4-iodo-3-nitrobenzoate is used as pharmaceutical intermediate.

Synthesis

67-56-1

35674-27-2

89976-27-2

Example 1: General procedure for the preparation of methyl 4-iodo-3-nitrobenzoate using methanol/sulfuric acid 1. dissolve 4-iodo-3-nitrobenzoic acid (3 g, 10 mmol) in methanol (30 ml) and cool the solution to 0°C. 2. sulfuric acid (3.4 g, 34.6 mmol) was added slowly to the above cooled solution. 3. the reaction mixture was gradually warmed to room temperature and subsequently heated to reflux (about 70 °C) and maintained for 8 hours. 4. Upon completion of the reaction, the reaction mixture was cooled and neutralized to pH neutral with solid NaHCO3 and filtered to remove the resulting salt. 5. The filtrate was concentrated under pressure to give a crude product. 6. Water (30 ml) was added to the crude product and extracted with methyl tertiary butyl ether (MTBE, 30 ml x 2). 7. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate and filtered. 8. The solvent was evaporated under pressure to give methyl 4-iodo-3-nitrobenzoate as a yellow solid (2.67 g, 85% yield, 98% HPLC purity).

References

[1] Dalton Transactions, 2015, vol. 44, # 5, p. 2047 - 2051
[2] Chemical Communications, 2017, vol. 53, # 55, p. 7808 - 7811
[3] Patent: US2013/172618, 2013, A1. Location in patent: Paragraph 0025
[4] Patent: WO2017/48954, 2017, A1. Location in patent: Paragraph 00095
[5] Patent: WO2005/40157, 2005, A2. Location in patent: Page/Page column 68

METHYL 4-IODO-3-NITROBENZOATESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006356688 18621169109
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INTATRADE GmbH
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+49 3493/605464
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Alfa Aesar
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Energy Chemical
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Shanghai Harvest Chemical Industrial Co., Ltd.
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sales@harvest-chem.com