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ChemicalBook--->CAS DataBase List--->33631-09-3

33631-09-3

33631-09-3 Structure

33631-09-3 Structure
IdentificationBack Directory
[Name]

3-AMINO-4-METHOXYPYRIDINE
[CAS]

33631-09-3
[Synonyms]

CBI-BB ZERO/004846
4-Methoxy-3-PyridinaMine
3-AMINO-4-METHOXYPYRIDINE
3-Pyridinamine, 4-methoxy-
4-METHOXY-PYRIDIN-3-YLAMINE
3-Amino-4-methoxypyridine ,98%
3-AMINO-4-METHOXYPYRIDINE ISO 9001:2015 REACH
[Molecular Formula]

C6H8N2O
[MDL Number]

MFCD07374959
[MOL File]

33631-09-3.mol
[Molecular Weight]

124.14
Chemical PropertiesBack Directory
[Melting point ]

83 °C
[Boiling point ]

270.4±20.0 °C(Predicted)
[density ]

1.139±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

solid
[pka]

7.48±0.18(Predicted)
[color ]

Brown
[InChI]

InChI=1S/C6H8N2O/c1-9-6-2-3-8-4-5(6)7/h2-4H,7H2,1H3
[InChIKey]

STWMPIWLSQKHSJ-UHFFFAOYSA-N
[SMILES]

C1=NC=CC(OC)=C1N
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P271-P261-P280
[Hazard Codes ]

Xn
[Risk Statements ]

22-20/21/22
[Safety Statements ]

36/37
[HS Code ]

29339900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4-Methoxy-3-nitropyridine-->Ethanol-->Hydrogen
[Preparation Products]

2-Bromo-3-fluoro-4-methoxypyridine
Hazard InformationBack Directory
[Chemical Properties]

Off-white solid
[Synthesis]

4-Methoxy-3-nitropyridine

31872-62-5

3-AMINO-4-METHOXYPYRIDINE

33631-09-3

Example 93: Synthesis of 4-hydroxy-4-[3-(trifluoromethyl)phenyl]piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-b]pyridin-2-yl)-amide; Step 1: To a solution of 4-methoxy-3-nitropyridine (5.0 g, 32.44 mmol) in ethanol (100 mL) was added 10% palladium/carbon catalyst (200 mg). The reaction mixture was placed under hydrogen atmosphere (50 psi) and the reaction was shaken at room temperature for 6 hours. The progress of the reaction was monitored by thin layer chromatography (TLC, 50% ethyl acetate/hexane) to confirm complete conversion of the feedstock. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated under reduced pressure to afford 3-amino-4-methoxypyridine (4.0 g, 32.44 mmol, 100% yield), the product was a dark red oil.

[References]

[1] Patent: US2007/270433, 2007, A1. Location in patent: Page/Page column 47
[2] Patent: WO2012/67664, 2012, A1. Location in patent: Page/Page column 53
[3] Inorganic Chemistry, 2013, vol. 52, # 7, p. 3653 - 3662
[4] Patent: US2011/9405, 2011, A1. Location in patent: Page/Page column 49-50
[5] Chemistry - A European Journal, 2012, vol. 18, # 51, p. 16358 - 16368
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-4-METHOXYPYRIDINE(33631-09-3)1HNMR
3-AMINO-4-METHOXYPYRIDINE(33631-09-3)1HNMR
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