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867012-70-2

867012-70-2 Structure

867012-70-2 Structure
IdentificationBack Directory
[Name]

5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL
[CAS]

867012-70-2
[Synonyms]

3-Amino-6-methoxy-5-methyL
5-AMINO-2-METHOXY-3-PICOLINE HCL
6-methoxy-5-methylpyridin-3-amine
6-Methoxy-5-methyl-3-pyridinamine
2-methoxy-3-methyl-5-aminopyridine
3-Amino-6-methoxy-5-methylpyridine
3-Pyridinamine, 6-methoxy-5-methyl-
5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL
3-Amino-6-methoxy-5-methylpyridine 97%
5-AMINO-2-METHOXY-3-PICOLINE HYDROCHLORIDE
5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL ISO 9001:2015 REACH
6-Methoxy-5-me6-Methoxy-5-methylpyridin-3-aminethylpyridin-3-amine
[Molecular Formula]

C7H10N2O
[MDL Number]

MFCD05662388
[MOL File]

867012-70-2.mol
[Molecular Weight]

138.17
Chemical PropertiesBack Directory
[Melting point ]

53-57°C
[Boiling point ]

268℃
[density ]

1.103
[Fp ]

116℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

4.62±0.20(Predicted)
[Appearance]

Pale purple to purple Powder
[InChI]

1S/C7H10N2O/c1-5-3-6(8)4-9-7(5)10-2/h3-4H,8H2,1-2H3
[InChIKey]

RFEMLHVKBYMWAM-UHFFFAOYSA-N
[SMILES]

COc1ncc(N)cc1C
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL(867012-70-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Methoxy-5-nitro-3-picoline

89694-10-0

5-AMINO-2-METHOXY-3-METHYLPYRIDINE HCL

867012-70-2

General procedure for the synthesis of 3-amino-6-methoxy-5-methylpyridine from 2-methoxy-5-nitro-3-methylpyridine: (1c) 6-methoxy-5-methyl-3-pyridinamine [Eq. 10]; 2-methoxy-3-methyl-5-nitro-pyridine (1.63 g, 9.71 mmol) was dissolved in methanol (50 mL), 10% Pd/C catalyst was added (50% water content, 800 mg) and the reaction was stirred under hydrogen atmosphere for 2 h 10 min. Upon completion of the reaction, it was filtered through diatomaceous earth and the solvent was evaporated to afford 3-amino-6-methoxy-5-methylpyridine (1.25 g, 9.0 mmol, 93% yield) as a blue oil.1H NMR (400 MHz, DMSO-d6) δ ppm: 2.03 (3H, s), 3.73 (3H, s), 4.62 (2H, s), and 6.83-6.86 (1H, m), 7.31-7.34 (1H, m).

[References]

[1] Patent: WO2005/103049, 2005, A1. Location in patent: Page/Page column 63-64
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3056 - 3062
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