7579-20-6

  • Product Name:3-Amino-4-Pyridinecarboxylic Acid
  • Molecular Formula:C6H6N2O2
  • Purity:99%
  • Molecular Weight:138.126
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Product Details;

CasNo: 7579-20-6

Molecular Formula: C6H6N2O2

Appearance: light yellow crystalline

Manufacturer supply top purity 3-Amino-4-Pyridinecarboxylic Acid 7579-20-6 with ISO standards

  • Molecular Formula:C6H6N2O2
  • Molecular Weight:138.126
  • Appearance/Colour:light yellow crystalline 
  • Vapor Pressure:1.06E-10mmHg at 25°C 
  • Melting Point:300 °C 
  • Boiling Point:497.1 °C at 760 mmHg 
  • PKA:2.69±0.10(Predicted) 
  • Flash Point:254.4 °C 
  • PSA:76.21000 
  • Density:1.417 g/cm3 
  • LogP:0.94320 

3-Aminoisonicotinic acid(Cas 7579-20-6) Usage

InChI:InChI=1/C6H6N2O2/c7-5-3-8-2-1-4(5)6(9)10/h1-3H,7H2,(H,9,10)/p-1

7579-20-6 Relevant articles

TRICYCLIC HETEROARYL COMPOUNDS USEFUL AS IRAK4 INHIBITORS

-

Page/Page column 51-52, (2021/02/12)

Disclosed are compounds of Formula (I) o...

Selenium-catalyzed intramolecular atom- And redox-economical transformation ofo-nitrotoluenes into anthranilic acids

Jiang, Xuefeng,Li, Yiming,Lin, Zhenyang,Wang, Yuhong,Yang, Tilong

supporting information, p. 2986 - 2991 (2021/05/05)

Anthranilic acids (AAs) are significant ...

Anthranilic acid and derivatives thereof as well as synthesis method and application thereof

-

Paragraph 0113-0115, (2021/09/15)

In the reaction solvent, o-methyl (heter...

Synthesis method of 3-amino methyl isonicotinate

-

, (2021/09/15)

The invention discloses a synthesis meth...

7579-20-6 Process route

cinchomeronic anhydride
4664-08-8

cinchomeronic anhydride

3-Aminopyridine-4-carboxylic acid
7579-20-6

3-Aminopyridine-4-carboxylic acid

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: MeCONH2 / Heating
2: 69 percent / Br2 / aq. NaOH / 80 °C
With acetamide; bromine; In sodium hydroxide;
 
3,4-pyridinedicarboximide
4664-01-1

3,4-pyridinedicarboximide

3-Aminopyridine-4-carboxylic acid
7579-20-6

3-Aminopyridine-4-carboxylic acid

Conditions
Conditions Yield
With bromine; sodium hydroxide; In water; at 90 ℃; for 0.666667h; Cooling with ice;
100%
With sodium hydroxide; bromine; at 85 ℃; for 0.333333h;
79%
With bromine; sodium hydroxide; In water; at 0 - 80 ℃; for 8h;
72%
With sodium hydroxide; bromine; at 80 ℃; for 0.166667h;
70%
With bromine; In sodium hydroxide; at 80 ℃;
69%
3,4-pyridinedicarboximide; With sodium hydroxide; bromine; In water; at 7 - 80 ℃; for 0.5h;
With acetic acid; In water; at 37 ℃; pH=5.5;
68.33%
3,4-pyridinedicarboximide; With sodium hydroxide; bromine; In water; at 0 - 80 ℃; for 0.75h;
With acetic acid; In water;
67%
3,4-pyridinedicarboximide; With sodium hydroxide; bromine; In water; at 80 ℃; for 1.1667h;
With acetic acid; In water; at 20 ℃; for 0.166667h;
64%
With sodium hydroxide; bromine; In water; at 0 - 80 ℃; for 0.75h;
62%
With bromine; sodium hydroxide; In water; at 0 - 85 ℃; for 1.25h;
62%
With bromine; In sodium hydroxide;
57%
3,4-pyridinedicarboximide; With sodium hydroxide; bromine; In water; at 7 - 85 ℃; for 1.5h;
With acetic acid; In water; at 20 - 30 ℃;
57%
With bromine; In sodium hydroxide;
57%
3,4-pyridinedicarboximide; With sodium hydroxide; bromine; In water; at 7 ℃;
at 80 - 85 ℃; for 0.75h;
With acetic acid; at 37 ℃; pH=5.5;
 
With sodium hydroxide; bromine; In water; at 0 - 85 ℃; for 0.75h;
 

7579-20-6 Upstream products

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7579-20-6 Downstream products

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