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219312-44-4

219312-44-4 Structure

219312-44-4 Structure
IdentificationBack Directory
[Name]

2-AMINO-4-CHLORO-6-NITROTOLUENE
[CAS]

219312-44-4
[Synonyms]

2-AMINO-4-CHLORO-6-NITROTOLUENE
5-Chloro-2-Methyl-3-nitroaniline
2-amino-4-chloro-7-nitro-toluene
5-chloro-2-methyl-3-nitrobenzenamine
Benzenamine, 5-chloro-2-methyl-3-nitro-
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C7H7ClN2O2
[MDL Number]

MFCD01109853
[MOL File]

219312-44-4.mol
[Molecular Weight]

186.6
Chemical PropertiesBack Directory
[Boiling point ]

333.4±37.0 °C(Predicted)
[density ]

1.415±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

1.08±0.10(Predicted)
[Appearance]

Yellow to orange Solid
Safety DataBack Directory
[HS Code ]

2921490090
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-4-CHLORO-6-NITROTOLUENE(219312-44-4)1HNMR
2-AMINO-4-CHLORO-6-NITROTOLUENE(219312-44-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-IODO-2,6-DINITROTOLUENE

35572-79-3

2-AMINO-4-CHLORO-6-NITROTOLUENE

219312-44-4

4-Iodo-2,6-dinitrotoluene (5.9 g, 23.60 mmol) was used as raw material and dissolved in a solvent mixture of methanol (10 mL) and 1,4-dioxane (5 mL). Under ice bath cooling conditions, 10 N hydrochloric acid (12 mL) and iron powder (3.96 g, 70.80 mmol) were slowly added. The reaction mixture was stirred at 80 °C for 3 h. The progress of the reaction was monitored by thin layer chromatography (TLC) until complete conversion of the feedstock. Upon completion of the reaction, 3.55 g of the light yellow powdery product 2-amino-4-chloro-6-nitrotoluene was obtained in 68.4% yield.

[References]

[1] Patent: CN108689937, 2018, A. Location in patent: Paragraph 0069; 0070; 0073; 0074
[2] Patent: CN108689936, 2018, A. Location in patent: Paragraph 0070; 0072; 0076; 0077
[3] Patent: US2010/63066, 2010, A1. Location in patent: Page/Page column 36
[4] Journal of the Chemical Society, 1905, vol. 87, p. 1265
[5] Patent: US5952362, 1999, A
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