ChemicalBook--->CAS DataBase List--->18344-51-9

18344-51-9

18344-51-9 Structure

18344-51-9 Structure
IdentificationMore
[Name]

2-Amino-3-methyl-5-nitropyridine
[CAS]

18344-51-9
[Synonyms]

2-AMINO-3-METHYL-5-NITROPYRIDINE
2-AMINO-5-NITRO-3-PICOLINE
3-METHYL-5-NITROPYRIDIN-2-AMINE
3-METHYL-5-NITRO-PYRIDIN-2-YLAMINE
3-METHYL-5-NITRO-PYRIDINE-2-YLAMINE
TIMTEC-BB SBB005535
2-Bromo-5-Nitro-3-Methyl Pyridine
3-Methyl-5-nitro-pyridin-2-ylamin
2-Amino-5-nitro-3-methylpyridine
2-AMINO-5-NITRO-3-PICOLINE (2-AMINO-3-METHYL-5-NITROPYRIDINE)
2-Amino-3-methyl-5-nitropyridine ,98%
3-Methyl-5-nitro-2-pyridinamine
3-Methyl-5-nitropyridine-2-amine
[EINECS(EC#)]

623-204-7
[Molecular Formula]

C6H7N3O2
[MDL Number]

MFCD03095060
[Molecular Weight]

153.14
[MOL File]

18344-51-9.mol
Chemical PropertiesBack Directory
[Appearance]

White to yellow crystalline powder.
[Melting point ]

256-260 °C
[Boiling point ]

276.04°C (rough estimate)
[density ]

1.3682 (rough estimate)
[refractive index ]

1.6500 (estimate)
[storage temp. ]

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

powder to crystal
[pka]

3.13±0.49(Predicted)
[color ]

Light yellow to Yellow to Orange
[Detection Methods]

HPLC
[BRN ]

126947
[InChI]

InChI=1S/C6H7N3O2/c1-4-2-5(9(10)11)3-8-6(4)7/h2-3H,1H3,(H2,7,8)
[InChIKey]

JLPYUDJJBGYXEZ-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=C([N+]([O-])=O)C=C1C
[CAS DataBase Reference]

18344-51-9(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

2-Amino-3-methyl-5-nitropyridine is a pyridine derivative that can be used as a pharmaceutical intermediate.
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R41:Risk of serious damage to eyes.
R22:Harmful if swallowed.
[Safety Statements ]

S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S22:Do not breathe dust .
S39:Wear eye/face protection .
S36:Wear suitable protective clothing .
[RIDADR ]

UN2811
[WGK Germany ]

1
[HazardClass ]

IRRITANT
[HS Code ]

29333990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Sulfuric acid-->Nitric acid-->Chloroform-->Sodium sulfate-->Sodium chloride-->2-Amino-3-picoline-->3-Methyl-N-nitropyridin-2-amine-->Pyrimidine, 2-ethyl-5-nitro- (9CI)-->3-METHYL-5-NITROPYRIDINE-->propionamidine hydrochloride-->Pyrimidine, 5-nitro- (8CI,9CI)
Hazard InformationBack Directory
[Chemical Properties]

White to yellow crystalline powder.
[Synthesis]

2-Amino-3-picoline

1603-40-3

2-Amino-3-methyl-5-nitropyridine

18344-51-9

The general procedure for the synthesis of 2-amino-3-methyl-5-nitropyridine from 2-amino-3-methylpyridine was as follows: 3-methylpyridin-2-amine (5.0 g, 46.2 mmol) was dissolved in concentrated sulfuric acid (24 mL) and the mixture was cooled to 0 °C. At the same time, fuming nitric acid (density = 1.5, 3.5 mL) was cooled to 0 °C. Concentrated sulfuric acid (3.5 mL) was slowly added dropwise to the reaction mixture while keeping the temperature below 20°C. Subsequently, the stirred mixture was gradually warmed to 20 °C and transferred to a second flask in 3-5 mL batches. The second flask was heated to 35-40°C (note: the temperature should not exceed 40°C and the temperature should be carefully monitored after each addition of a new batch). Next, the reaction mixture was continued to be stirred at 50°C for 30 minutes. Once the reaction is complete, the mixture is cooled to room temperature and neutralized with concentrated ammonia. At this point, a precipitate is generated, which is filtered and washed sequentially with water and 50% aqueous DMFA (6 mL). Finally, the product was purified by recrystallization from DMFA to give 3-methyl-5-nitropyridin-2-amine (2.52 g, 35% yield).

[References]

[1] Patent: EP1894924, 2008, A1. Location in patent: Page/Page column 36
[2] Journal of Organic Chemistry, 1949, vol. 14, p. 328,331
[3] Journal of the American Chemical Society, 1955, vol. 77, p. 3154
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-methyl-5-nitropyridine(18344-51-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Amino-5-nitro-3-picoline, 98%(18344-51-9)
[Alfa Aesar]

2-Amino-3-methyl-5-nitropyridine, 97%(18344-51-9)
[Sigma Aldrich]

18344-51-9(sigmaaldrich)
[TCI AMERICA]

2-Amino-3-methyl-5-nitropyridine,>98.0%(GC)(T)(18344-51-9)
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