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Home > Encyclopedia > 2-Amino-3-methyl-5-nitropyridine

2-Amino-3-methyl-5-nitropyridine

2-Amino-3-methyl-5-nitropyridine structure

2-Amino-3-methyl-5-nitropyridine 

structure
  • CAS No:

    18344-51-9

  • Formula:

    C6H7N3O2

  • Chemical Name:

    2-Amino-3-methyl-5-nitropyridine

  • Synonyms:

    2-AMINO-3-METHYL-5-NITROPYRIDINE;2-AMINO-5-NITRO-3-PICOLINE;3-METHYL-5-NITRO-PYRIDINE-2-YLAMINE;3-METHYL-5-NITROPYRIDIN-2-AMINE;3-METHYL-5-NITRO-PYRIDIN-2-YLAMINE;TIMTEC-BB SBB005535;2-Bromo-5-Nitro-3-Methyl Pyridine;3-Methyl-5-nitro-pyridin-2-ylamin

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

White to yellow crystalline powder.

2-Amino-3-methyl-5-nitropyridine Basic Attributes

153.14

153.053833

126947

1312995-182-4

DTXSID80370314

29333990

Characteristics

84.7

0.7

White to yellow crystalline powder.

1.3682 (rough estimate)

249-253 °C

276.04°C (rough estimate)

173.6±26.5 °C

1.6500 (estimate)

Room temperature.

1.8E-05mmHg at 25°C

Safety Information

IRRITANT

UN2811

1

36/37/38-20/21/22-41-22

36/37/39-26-22-39-36-37

Xn,Xi

P280-P305 + P351 + P338

H302-H318

|Danger|H302 (88.64%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Amino-3-methyl-5-nitropyridine Use and Manufacturing

3-Methyl-pyridin-2-ylamine (5.0 g, 46.2 mmol) was dissolved in concentrated sulfuric acid (24ml), the mixture was chilled to 0°C and a mixture of fuming nitric acid (d=1.5, 3.5ml) and concentrated sulfuric acid (3.5ml) was added dropwise to the reaction mixture while temperature was kept below 20°C. 3-Methyl-pyridin-2-ylamine (5.0 g, 46.2 mmol) was dissolved in concentrated sulfuric acid (24ml), the mixture was chilled to 0C and a mixture of fuming nitric acid (d=1.5, 3.5ml) and concentrated sulfuric acid (3.5ml) was added dropwise to the reaction mixture while temperature was kept below 20C. The stirred mixture was allowed to warm to 20C and transferred in portions of 3-5ml into a second flask which was heated to 35-40C (the temperature was not allowed to rise over 40C - monitoring carefully the temperature after every addition of a new portion). The resulting reaction mixture was subsequently stirred for additional 30min at 50C, cooled to ambient temperature and neutralized with concentrated aqueous ammonia. This led to the formation of a precipitated which was filtered, washed with water and aqueous DMFA (50%, 6ml), and recrystallized from DMFA yielding

Computed Properties

Molecular Weight:153.14
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Exact Mass:153.053826475
Monoisotopic Mass:153.053826475
Topological Polar Surface Area:84.7
Heavy Atom Count:11
Complexity:156
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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