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Home > Chemical Reagents > Organic Reagents > 5-Bromo-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester for Sale > 5-Bromo-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester
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5-Bromo-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester buy - image1

5-Bromo-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester

Unit Price:

$70-80/G FOB

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CAS No.:

105544-30-7

Grade:

Industrial Grade

Content:

98%

Port:

guanghzou

Brand:

Cuicheng Bio

Packaging:

g/kg

Price valid (until):

2026-07-02

Company Type:
Manufactory
Location:
China
Qualification:
Main Products:

Ginsenoside Rb1,Ginsenoside Rg1,Ginsenoside Re,Ginsenoside CK,Ginsenoside Rg2,Ginsenoside Rg5

  • Product Description

  • Seller Information

  • Description
    5-Bromo-1H-pyrazolo[3,4-c]pyridine functions primarily as a highly valuable heterocyclic core scaffold and pharmaceutical intermediate in modern drug discovery, particularly in Fragment-Based Drug Discovery (FBDD). Its core roles in organic synthesis and drug design can be detailed as follows:
    1. Core Scaffold for Kinase Inhibitor Design
    The bicyclic system (a pyrazole ring fused with a pyridine ring) highly mimics the core structure of natural purines or other bio-active molecules. In medicinal chemistry, it is widely utilized to develop kinase inhibitors targeting malignancies, such as compounds targeting oncogenic or immunodeficient-related proteins like ERK2, Pim kinases, or Protein Kinase B (PKB).
    2. Precise Vectorial Functionalization
    According to literature in chemical journals, this compound possesses excellent potential for late-stage multi-site chemical modification. It allows researchers to extend side chains into different spatial directions (growth vectors) while maintaining the core scaffold:
    • The C-5 Position (Bromine-substituted site): This is the most critical functional site of the molecule. Through transition-metal-catalyzed Buchwald–Hartwig amination or Suzuki–Miyaura cross-coupling reactions, the bromine atom can be efficiently replaced with diverse aryl or amino groups to significantly enhance target affinity.
    • The N-1 and N-2 Positions (Pyrazole nitrogens): These sites can be selectively modified via protection reactions or N-alkylation to balance the lipophilicity and metabolic stability of the final drug molecule.
    • The C-3 Position: Advanced groups can be introduced through tandem borylation.
    3. Rapid Evolution from "Fragment" to "Lead Compound"
    In the pharmaceutical industry and biochemical laboratories, it is treated as a highly efficient building block. Instead of synthesizing the complex bicyclic ring from scratch, medicinal chemists leverage the reactivity of its various positions to rapidly construct diverse chemical libraries. This drastically shortens the R&D cycle from initial fragment hits to optimized lead compounds.


    Items Specifications






    Basic Info
    Product Name:

    5-Bromo-3-nitro-pyridin-2-yloxy)-acetic acid ethyl ester

    Other Name:

    Ethyl 2-((5-bromo-3-nitropyridin-2-yl)oxy)acetate;Ethyl 2-[(5-Bromo-3-nitro-2-pyridyl)oxy]acetate;ETHYL 2-(5-BROMO-3-NITROPYRIDIN-2-YLOXY)ACETATE;ethyl 2-(5-bromo-3-nitropyridin-2-yl)oxyacetate;ETHYL 2-[(5-BROMO-3-NITROPYRIDIN-2-YL)OXY]ACETATE;C9H9BrN2O5;SCHEMBL751950;CTK8C2150;KS-00000QGU;ZINC5585673

    CAS No.:

    105544-30-7

    Molecular Formula:

    C9H9BrN2O5

    InChIKeys:

    UHIILDDDMFTHKM-UHFFFAOYSA-N

    Molecular Weight:

    305.083

    Exact Mass:

    303.969482

    HScode:

    2933399090

    Categories:

    Organic Reagents

    Characteristics
    PSA:

    94.2

    XLogP3:

    2

    Density:

    1.6±0.1 g/cm3

    Boiling Point:

    364.1°C at 760 mmHg

    Flash Point:

    174.0±26.5 °C

    Refractive Index:

    1.563

    Hazard Identification

    Classification of the substance or mixture

    no data available

    GHS label elements, including precautionary statements

    Pictogram(s) no data available
    Signal word

    no data available

    Hazard statement(s)

    no data available

    Precautionary statement(s)
    Prevention

    no data available

    Response

    no data available

    Storage

    no data available

    Disposal

    no data available

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Manufactory

    Main Products:

    Ginsenoside Rb1,Ginsenoside Rg1,Ginsenoside Re,Ginsenoside CK,Ginsenoside Rg2,Ginsenoside Rg5

    Location:

    Chuangzhi valley,Chuangzhi Industrial Park ,Hanzhong Economic and Technological Dvelopment Zone,Hanzhong City, Shaanxi Province

    Year of Establishment:

    2019

  • Country Product Purchase Quantity Date Posted
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