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Home > Encyclopedia > 5-Bromo-6-methyl-2-pyridinamine

5-Bromo-6-methyl-2-pyridinamine

5-Bromo-6-methyl-2-pyridinamine structure

5-Bromo-6-methyl-2-pyridinamine 

structure
  • CAS No:

    42753-71-9

  • Formula:

    C6H7BrN2

  • Chemical Name:

    5-Bromo-6-methyl-2-pyridinamine

  • Synonyms:

    2-Pyridinamine,5-bromo-6-methyl-;5-Bromo-6-methyl-2-pyridinamine;2-Amino-5-bromo-6-methylpyridine;6-Amino-3-bromo-2-picoline;6-Amino-3-bromo-2-methylpyridine;3-Bromo-2-methylpyridin-6-amine;5-Bromo-6-methylpyridin-2-amine;5-Bromo-6-methyl-2-aminopyridine;2-Amino-6-methyl-5-bromopyridine

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Light yellow Cryst

5-Bromo-6-methyl-2-pyridinamine Basic Attributes

187.04

187.04

114140

255-927-5

DTXSID8068414

29333999

Characteristics

38.9

1.6

White to off-white Fluffy Powder

1.6±0.1 g/cm3

79-84 °C(lit.)

234.3°C at 760 mmHg

95.5±25.9 °C

1.617

Safety Information

IRRITANT

NONH for all modes of transport

3

36/37/38

26-36-26/37/39

Xi

Irritant

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

5-Bromo-6-methyl-2-pyridinamine Use and Manufacturing

Methods of Manufacturing

General procedure: To a mixture of 2-aminopyridine (0.5 mmol, 1 equiv), p-TSA (0.4 mmol, 0.8 equiv), 1-butylpyridinium bromide (1.5 mmol, 3 equiv) in a 50 mL Schlenk tube were added 1, 2-dimethoxyethane (2 mL) under air. Then HTo a 2L flask was added 2-amino-6-methylpyridine (50 g, 0.462 mole) and DCM (1.0 L) and the solution was cooled to -5 Step 1 The 6-Methylpyridin-2-amine (1.08g, 10mmol) dissolved in glacial acetic acid (20 ml) in, bromine is added for (1.6g, 10mmol), 25 °C reaction 16 hours. Water (50 ml), ethyl acetate extraction (150 ml × 2), combined organic phase, saturated salt water washing, dry anhydrous sodium sulfate, concentrated under vacuum, the crude product by silica gel column chromatography (petroleum ether: ethyl acetate = 3:1) purification, to obtain the title compound (800 mg, yield 42.8percent).A solution of 6-methylpyridin-2-amine (5 g 46.2 mmol) in MeOH (20 mL) stirred under N

2-Pyridinamine, 5-bromo-6-methyl-: INACTIVE

Computed Properties

Molecular Weight:187.04
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:185.97926
Monoisotopic Mass:185.97926
Topological Polar Surface Area:38.9
Heavy Atom Count:9
Complexity:97.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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