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4-Hydroxy-5-azaindole is a heterocyclic aromatic compound with the molecular formula C7H6N2O and a molecular weight of 134.14 g/mol. It features a pyridine ring with a hydroxyl group at the 4-position and an indole ring system. 4-Hydroxy-5-azaindole is recognized for its fluorescent properties and is utilized as a building block in organic synthesis and pharmaceutical research, with potential applications in enzyme inhibition and as a pharmaceutical intermediate for drug synthesis.

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  • 54415-77-9 Structure
  • Basic information

    1. Product Name: 4-HYDROXY-5-AZAINDOLE
    2. Synonyms: 4-HYDROXY-5-AZAINDOLE;1,5-Dihydro-4H-pyrrolo[3,2-c]pyridin-4-one;1H-Pyrrolo[3,2-c]pyridin-4(5H)-one;4,5-dihydro-4-oxo-1H-pyrrolo[3,2-c]pyridine;4H-Pyrrolo[3,2-c]pyridin-4-one, 1,5-dihydro-
    3. CAS NO:54415-77-9
    4. Molecular Formula: C7H6N2O
    5. Molecular Weight: 134.13534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54415-77-9.mol
  • Chemical Properties

    1. Melting Point: 242-244 °C
    2. Boiling Point: 486.2 °C at 760 mmHg
    3. Flash Point: 247.8 °C
    4. Appearance: /
    5. Density: 1.335 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 13.27±0.20(Predicted)
    10. CAS DataBase Reference: 4-HYDROXY-5-AZAINDOLE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-HYDROXY-5-AZAINDOLE(54415-77-9)
    12. EPA Substance Registry System: 4-HYDROXY-5-AZAINDOLE(54415-77-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 54415-77-9(Hazardous Substances Data)

54415-77-9 Usage

Uses

Used in Organic Synthesis:
4-Hydroxy-5-azaindole is used as a building block for the synthesis of various organic compounds due to its unique structure and reactivity.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Hydroxy-5-azaindole is used as a research compound for studying its potential biological activities, such as its role as an enzyme inhibitor.
Used in Drug Synthesis:
4-Hydroxy-5-azaindole serves as a pharmaceutical intermediate, contributing to the development of new drugs through its incorporation into their molecular structures.
Used in Biochemical and Biomedical Applications:
Leveraging its fluorescent properties, 4-Hydroxy-5-azaindole is utilized in biochemical and biomedical applications for imaging, detection, and analysis purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 54415-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,1 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54415-77:
(7*5)+(6*4)+(5*4)+(4*1)+(3*5)+(2*7)+(1*7)=119
119 % 10 = 9
So 54415-77-9 is a valid CAS Registry Number.
InChI:InChI:1S/C7H6N2O/c10-7-5-1-3-8-6(5)2-4-9-7/h1-4,8H,(H,9,10)

54415-77-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[3,2-c]pyridin-4(5H)-one

1.2 Other means of identification

Product number -
Other names 1,5-dihydropyrrolo[3,2-c]pyridin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54415-77-9 SDS

54415-77-9Relevant articles and documents

Synthesis of Pyrrolopyridines (Azaindoles)

Mahadevan,Indumathy,Rasmussen, Malcolm

, p. 359 - 367 (2007/10/02)

Improved, convenient, and reliable routes for synthesis of 4-,5-,6-, and 7-azaindole, 7-methyl-4-azaindole, 7-methyl-6-azaindole, and the hithero unreported 7-amino-4-azaindole are described.The syntheses have been accomplished either by significant modifications to established procedures or by new methods with afford the compounds in improved yields.

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