1000339-23-0

  • Product Name:2-Amino-5-bromoisonicotinic acid
  • Molecular Formula:C6H5BrN2O2
  • Molecular Weight:217.0201
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Product Details

Purity:99%

Reliable factory customized supply 2-Amino-5-bromoisonicotinic acid 1000339-23-0

  • Molecular Formula:C6H5BrN2O2
  • Molecular Weight:217.0201
  • Boiling Point:464.1 °C at 760 mmHg 
  • PKA:1.16±0.10(Predicted) 
  • Flash Point:234.5 °C 
  • PSA:76.21000 
  • Density:1.909 g/cm3 
  • LogP:1.70570 

2-Amino-5-bromoisonicotinic acid(Cas 1000339-23-0) Usage

General Description

2-Amino-5-bromoisonicotinic acid is a specialized chemical compound that carries the molecular formula C6H5BrN2O2. It is categorized as an isonicotinic acid, which belongs to a class of organic compounds known as pyridinecarboxylic acids. This specific compound is recognized for its uses in various types of chemical and pharmaceutical research due to the unique properties it holds. It is characterized by its bromo and amino substituents which can interact in reactions, giving it utility as a building block or precursor in various types of synthesis. As with many chemicals, it should be handled with care due to potential risks upon contact or ingestion. It is notable for being an advanced intermediate in the synthesis of more complex molecules.

InChI:InChI=1/C6H5BrN2O2/c7-4-2-9-5(8)1-3(4)6(10)11/h1-2H,(H2,8,9)(H,10,11)

1000339-23-0 Relevant articles

INHIBITORS OF HEPATITIS C VIRUS

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Page/Page column 145, (2012/05/19)

A class of compounds that inhibit Hepati...

1000339-23-0 Process route

methyl 2-amino-5-bromo-pyridine-4-carboxylate
882499-87-8

methyl 2-amino-5-bromo-pyridine-4-carboxylate

C<sub>6</sub>H<sub>5</sub>BrN<sub>2</sub>O<sub>2</sub>
1000339-23-0

C6H5BrN2O2

Conditions
Conditions Yield
methyl 2-amino-5-bromopyridine-4-carboxylate; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 70 ℃; for 2h; Inert atmosphere;
With hydrogenchloride; In tetrahydrofuran; methanol; water; at 0 ℃; pH=6;
83%
C<sub>6</sub>H<sub>5</sub>BrN<sub>2</sub>O<sub>2</sub>
1000339-23-0

C6H5BrN2O2

C<sub>20</sub>H<sub>19</sub>BrFN<sub>3</sub>O<sub>4</sub>
1374233-70-1

C20H19BrFN3O4

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: diphenyl phosphoryl azide; triethylamine / 6 h / 90 °C / Inert atmosphere
2.1: N,N-dimethyl-formamide / 42 h / 80 °C / Inert atmosphere
2.2: 0.25 h / 0 °C
With diphenyl phosphoryl azide; triethylamine; In N,N-dimethyl-formamide;

1000339-23-0 Upstream products

  • 882499-87-8
    882499-87-8

    methyl 2-amino-5-bromo-pyridine-4-carboxylate

1000339-23-0 Downstream products

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    1374233-70-1

    C20H19BrFN3O4

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    1374233-71-2

    C15H11BrFN3O2

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    1374233-72-3

    C17H15BrFN3O6S2

  • 1374233-73-4
    1374233-73-4

    C16H13BrFN3O4S