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1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI), also known as kynurenic acid, is a chemical compound with the molecular formula C7H4N2O2. It is a naturally occurring metabolite of the amino acid tryptophan, found in the human body and various foods such as meat and dairy products. 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI) has garnered interest due to its potential neuroprotective and anti-inflammatory properties, as well as its involvement in a range of physiological and pathological processes.

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  • 153072-89-0 Structure
  • Basic information

    1. Product Name: 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI)
    2. Synonyms: 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI);1H-Pyrrolo[3,2-b]pyridine-2,3-dione
    3. CAS NO:153072-89-0
    4. Molecular Formula: C7H4N2O2
    5. Molecular Weight: 148.12
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 153072-89-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.469
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: DMSO (Slightly), Methanol (Slightly, Sonicated), Water (Slightly, Sonicated)
    9. PKA: 8.30±0.20(Predicted)
    10. Stability: Hygroscopic
    11. CAS DataBase Reference: 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI)(153072-89-0)
    13. EPA Substance Registry System: 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI)(153072-89-0)
  • 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: 153072-89-0(Hazardous Substances Data)

153072-89-0 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI) is used as a potential therapeutic target for treating neurological disorders and inflammatory conditions. Its neuroprotective and anti-inflammatory properties make it a promising candidate for the development of new drugs to address these health issues.
Used in Nutritional Supplements:
Given its presence in certain foods and its potential health benefits, 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI) may also be used as an ingredient in nutritional supplements to support cognitive health and reduce inflammation.
Used in Research Applications:
In the field of scientific research, 1H-Pyrrolo[3,2-b]pyridine-2,3-dione(9CI) serves as an important chemical compound for studying the role of tryptophan metabolism in various biological processes and its implications in health and disease.

Check Digit Verification of cas no

The CAS Registry Mumber 153072-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153072-89:
(8*1)+(7*5)+(6*3)+(5*0)+(4*7)+(3*2)+(2*8)+(1*9)=120
120 % 10 = 0
So 153072-89-0 is a valid CAS Registry Number.

153072-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-pyrrolo[3,2-b]pyridine-2,3-dione

1.2 Other means of identification

Product number -
Other names 4-azaisatin

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:153072-89-0 SDS

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153072-89-0Downstream Products

153072-89-0Relevant articles and documents

Biphenyl-substituted quinoline derivatives

-

, (2008/06/13)

Compounds of the formula wherein X, R1, R2, R3, R4, R5, R6, A, B, D and E are as defined herein. These compounds inhibit the action of angiotensin II and are useful, therefore, for example, as antihypertensive agents.

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