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Home > Encyclopedia > 3-Methyl-4-pyridinamine

3-Methyl-4-pyridinamine

3-Methyl-4-pyridinamine structure

3-Methyl-4-pyridinamine 

structure
  • CAS No:

    1990-90-5

  • Formula:

    C6H8N2

  • Chemical Name:

    3-Methyl-4-pyridinamine

  • Synonyms:

    4-Pyridinamine,3-methyl-;3-Picoline,4-amino-;3-Methyl-4-pyridinamine;Phillips 1908;4-Amino-3-methylpyridine;3-Methyl-4-aminopyridine;4-Amino-3-picoline;NSC 52454;(3-Methylpyridin-4-yl)amine;3-Methylpyridin-4-amine

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Crystals

3-Methyl-4-pyridinamine Basic Attributes

108.14

108.14

217-872-5

52454

DTXSID90173676

29333999

Characteristics

38.9

0.5

0.9581 (rough estimate)

108-109 °C

192.78°C (rough estimate)

138.4±9.0 °C

1.5400 (estimate)

0.00918mmHg at 25°C

Oral-rat LD50: 446mg/kg; Oral-Bird LD50: 2.40 mg/kg

Flammable; burning produces toxic nitrogen oxide fumes

Safety Information

2811

23/24/25-36/37/38-34-22-20/21/22

22-36/37/39-45-36-27-26

TJ5140000

C,Xi,Xn

Warehouse ventilated, low temperature and dry

Harmful

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, and P501|Aggregated GHS information provided by 3 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

highly toxic

Drug Information

3-methyl-4-aminopyridine

3-Methyl-4-pyridinamine Use and Manufacturing

Step 2: A solution of 3-methyl-4-nitropyridine /V-oxide (30.0g, 195 mmol) and 10percent Pd-C (6.0 g) in EtOH (450 mL) was stirred at rt under H3-Methyl-4-nitropyridine 1-oxide (5.85 g) was dissolved in glacial acetic acid (115 mL) and hydrogenated in a Parr hydrogenation apparatus (catalyst: 220 mg Pt02 x 2 H20, 50 psi) at ambient temperature for 2.5 h. Then the catalyst was filtered off and the solvent was evaporated. After addition of 150 mL of water the pH was adjusted to 12 by addition of 2N NaOH. The resulting solution was extracted 10 times with 100 mL of dichloromethane (containing 5 percent methanol). The combined organic phases were dried over anhydrous sodium sulphate and evaporated to give 3.81 g (83.6percent) of 4-amino-3-methylpyridine.The crude 2-(5-chloro-2-fluorophenyl)-4-iodo-5, 6, 7, 8-tetrahydroquinazoline (130 mg, 0.35 mmol, 1 eq) was dissolved in dioxane (5 ml) and to this was added Pd(OAc)2 (4 mg, 0.02 mmol, 0.05 eq) followed by BINAP (16 mg, 0.03 mmol, 0.075 eq),

Computed Properties

Molecular Weight:108.14
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:108.068748264
Monoisotopic Mass:108.068748264
Topological Polar Surface Area:38.9
Heavy Atom Count:8
Complexity:72.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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