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Home > Encyclopedia > 3-AMINO-ISONICOTINIC ACID METHYL ESTER

3-AMINO-ISONICOTINIC ACID METHYL ESTER

3-AMINO-ISONICOTINIC ACID METHYL ESTER structure

3-AMINO-ISONICOTINIC ACID METHYL ESTER 

structure
  • CAS No:

    55279-30-6

  • Formula:

    C7H8N2O2

  • Chemical Name:

    3-AMINO-ISONICOTINIC ACID METHYL ESTER

  • Synonyms:

    METHYL 3-AMINOPYRIDINE-4-CARBOXYLATE;METHYL 3-AMINOISONICOTINATE;AKOS 93360;3-AMINO-ISONICOTINIC ACID METHYL ESTER;3-AMINO-4-PYRIDINECARBOXYLIC ACID METHYL ESTER;3-AMINOPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER;3-Amino-isonicotinic acid methyl ester ,98%;Tpc-py003

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Yellow powder

3-AMINO-ISONICOTINIC ACID METHYL ESTER Basic Attributes

152.15

152.058578

1592732-453-0

DTXSID70363396

2933399090

Characteristics

65.2

0.6

1.2±0.1 g/cm3

84-86

292.5°C at 760 mmHg

130.7±21.8 °C

1.571

>22.8 [ug/mL]

Safety Information

22-36/38

24/25

Xi,Xn

Irritant

P264, P270, P301+P312, P330, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory.

3-AMINO-ISONICOTINIC ACID METHYL ESTER Use and Manufacturing

(3. 55 g, 25. 7 mmol), H2SO4 (2. 5 ml) and methanol(50 ml) were heated at 80 C for 3 days. The methanol was evaporated, the residue diluted with water(75 ml) and heated to 80 C. Solid sodium carbonate was added until effervescence ceased. The mixture was cooled and extracted with dichloromethane (2 x 100 ml). The combined organic layers were dried overMgS04 and concentrated to give the title compound as a beige solid (2.36 g, 60 percent). 'H NMR (500 MHz, DMSO) 5 8.24 (1H, s), 7.74 (1H, d, J5. 3), 7.46 (1H, d, J5.2), 6.67 (2H, brs), 3.83 (3H, s). M/z (ES+) 153 (M+H+).Description 1 (3. 55 g, 25. 7 mmol), H2SO4 (2. 5 ml) and methanol(50 ml) were heated at 80 C for 3 days. The methanol was evaporated, the residue diluted with water(75 ml) and heated to 80 C. Solid sodium carbonate was added until effervescence ceased. The mixture was cooled and extracted with dichloromethane (2 x 100 ml). The combined organic layers were dried overMgS04 and concentrated to give the title compound as a beige solid (2.36 g, 60 percent). 'H NMR (500 MHz, DMSO) 5 8.24 (1H, s), 7.74 (1H, d, J5. 3), 7.46 (1H, d, J5.2), 6.67 (2H, brs), 3.83 (3H, s). M/z (ES+) 153 (M+H+).A mixture of 3-amino-isonicotinic acid (613 mg, 4.44 mmol), methanol (15 mL) and thionyl chloride (0.7 mL, 8.88 mmol) was stirred at reflux for 3 days.

Computed Properties

Molecular Weight:152.15
XLogP3:0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:152.058577502
Monoisotopic Mass:152.058577502
Topological Polar Surface Area:65.2
Heavy Atom Count:11
Complexity:149
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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