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1-Methyl-7-azaindole-5-carboxylic acid is a chemical compound with a molecular formula C10H8N2O2, belonging to the indole family and featuring a carboxylic acid group. It is a versatile building block in organic synthesis and has demonstrated potential in various applications, including pharmaceuticals, antimicrobial agents, and material development.

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  • 934568-20-4 Structure
  • Basic information

    1. Product Name: 1-Methyl-7-azaindole-5-carboxylic acid
    2. Synonyms: 1-Methyl-7-azaindole-5-carboxylic acid;1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 1-Methyl-;EOS-60339
    3. CAS NO:934568-20-4
    4. Molecular Formula: C9H8N2O2
    5. Molecular Weight: 176.17202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 934568-20-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Methyl-7-azaindole-5-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Methyl-7-azaindole-5-carboxylic acid(934568-20-4)
    11. EPA Substance Registry System: 1-Methyl-7-azaindole-5-carboxylic acid(934568-20-4)
  • 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: 934568-20-4(Hazardous Substances Data)

934568-20-4 Usage

Uses

Used in Pharmaceutical Industry:
1-Methyl-7-azaindole-5-carboxylic acid is used as a starting material for the synthesis of various bioactive molecules, contributing to the development of new drugs and therapeutic agents.
Used in Antimicrobial Applications:
1-Methyl-7-azaindole-5-carboxylic acid is used as an antimicrobial agent, exhibiting potential activity against a range of microorganisms, thereby contributing to the development of new antimicrobial treatments.
Used in Cancer Treatment Research:
1-Methyl-7-azaindole-5-carboxylic acid is used in research for its potential role in the treatment of cancer, as it has shown promise in targeting cancer cells and modulating relevant biological pathways.
Used in Material Development:
1-Methyl-7-azaindole-5-carboxylic acid is used in the development of new materials, leveraging its unique chemical properties to create innovative substances with potential applications in various industries.
Used in Organic Synthesis:
1-Methyl-7-azaindole-5-carboxylic acid is used as a key intermediate in organic synthesis, enabling the creation of a wide array of chemical compounds for diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 934568-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,5,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934568-20:
(8*9)+(7*3)+(6*4)+(5*5)+(4*6)+(3*8)+(2*2)+(1*0)=194
194 % 10 = 4
So 934568-20-4 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8N2O2/c1-11-3-2-6-4-7(9(12)13)5-10-8(6)11/h2-5H,1H3,(H,12,13)

934568-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylpyrrolo[2,3-b]pyridine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-METHYL-7-AZAINDOLE-5-CARBOXYLIC ACID

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:934568-20-4 SDS

934568-20-4Relevant articles and documents

PYRAZOLOPYRIMIDINES AS INHIBITORS OF GLUCOCORTICOID RECEPTOR TRANSLOCATION

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, (2016/08/23)

Provided herein are compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of Glucocorticoid Receptor (GR) translocation. Furthermore, the subject compounds and compositions are useful for the treatment of diseases involved in the hypothalamic-pituitary-adrenal (HPA) axis.

AMIDE COMPOUNDS, COMPOSITIONS AND APPLICATIONS THEREOF

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, (2015/03/16)

The present disclosure relates to substituted amide compounds that are inhibitors of Fatty Acid Amide Hydrolase (FAAH), their stereoisomers, tautomers, prodrugs, polymorphs, solvates, pharmaceutically acceptable salts, and pharmaceutical compositions cont

AMIDE COMPOUNDS, COMPOSITIONS AND APPLICATIONS THEREOF

-

, (2013/04/10)

The present disclosure relates to substituted amide compounds that are inhibitors of Fatty Acid Amide Hydrolase (FAAH), their stereoisomers, tautomers, prodrugs, polymorphs, solvates, pharmaceutically acceptable salts, and pharmaceutical compositions cont

Synthesis and evaluation of 5-fluoro-2-aryloxazolo[5,4- b ]pyridines as β-amyloid PET ligands and identification of MK-3328

Harrison, Scott T.,Mulhearn, James,Wolkenberg, Scott E.,Miller, Patricia J.,O'Malley, Stacey S.,Zeng, Zhizhen,Williams Jr., David L.,Hostetler, Eric D.,Sanabria-Bohorquez, Sandra,Gammage, Linda,Fan, Hong,Sur, Cyrille,Culberson, J. Christopher,Hargreaves, Richard J.,Cook, Jacquelynn J.,Hartman, George D.,Barrow, James C.

, p. 498 - 502 (2011/09/14)

5-Fluoro-2-aryloxazolo[5,4-b]pyridines were synthesized and investigated as potential 18F containing β-amyloid PET ligands. In competition binding assays using human AD brain homogenates, compounds 14b, 16b, and 17b were identified as having favorable potency versus human β-amyloid plaque and were radiolabeled for further evaluation in in vitro binding and in vivo PET imaging experiments. These studies led to the identification of 17b (MK-3328) as a candidate PET ligand for the clinical assessment of β-amyloid plaque load.

NOVEL SUBSTITUTED AZABENZOXAZOLES

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, (2010/01/12)

The present invention relates to novel amyloid binding compounds and methods for measuring effects of the compounds, by measuring changes of amyloid plaque level in living patients. More specifically, the present invention relates to a method of using the

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