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85414-82-0

2-Quinoxalinecarboxylicacid,3-amino-(9CI) is a chemical compound with the molecular formula C9H7N3O2. It is a derivative of quinoxaline, a heterocyclic compound containing a benzene ring fused to a pyrazine ring. The 3-amino substituent on the quinoxalinecarboxylic acid molecule gives it potential biological and pharmacological activity. 2-Quinoxalinecarboxylicacid,3-amino-(9CI) is of interest for its potential biological and pharmaceutical applications due to its unique structure and reactivity.

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  • 85414-82-0 Structure

  • Basic information

    1. Product Name: 2-Quinoxalinecarboxylicacid,3-amino-(9CI)
    2. Synonyms: 2-Quinoxalinecarboxylicacid,3-amino-(9CI);2-Quinoxalinecarboxylic acid, 3-aMino-;3-amino-2-Quinoxalinecarboxylic acid
    3. CAS NO:85414-82-0
    4. Molecular Formula: C9H7N3O2
    5. Molecular Weight: 189.17078
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 85414-82-0.mol

  • Chemical Properties

    1. Melting Point: 204 °C
    2. Boiling Point: 377.4 °C at 760 mmHg
    3. Flash Point: 182 °C
    4. Appearance: /
    5. Density: 1.515 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. PKA: 4.68±0.48(Predicted)
    10. CAS DataBase Reference: 2-Quinoxalinecarboxylicacid,3-amino-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Quinoxalinecarboxylicacid,3-amino-(9CI)(85414-82-0)
    12. EPA Substance Registry System: 2-Quinoxalinecarboxylicacid,3-amino-(9CI)(85414-82-0)

  • 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: 85414-82-0(Hazardous Substances Data)

85414-82-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Quinoxalinecarboxylicacid,3-amino-(9CI) is used as a pharmaceutical agent for its potential anti-cancer or anti-inflammatory properties. Its ability to interact with biological systems makes it a promising candidate for the development of new drugs targeting various diseases.
Used in Chemical Synthesis:
2-Quinoxalinecarboxylicacid,3-amino-(9CI) is used as a building block in the synthesis of other compounds with various pharmacological activities. Its unique structure and reactivity allow for the creation of novel compounds with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 85414-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,1 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85414-82:
(7*8)+(6*5)+(5*4)+(4*1)+(3*4)+(2*8)+(1*2)=140
140 % 10 = 0
So 85414-82-0 is a valid CAS Registry Number.

85414-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoquinoxaline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-AMINOQUINOXALINE-2-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:85414-82-0 SDS

85414-82-0Relevant articles and documents

Synthesis of new quinoxaline derivatives

Laskina,Mel'Nikova,Tselinskii

experimental part, p. 278 - 283 (2012/06/01)

Proceeding from 2-aminoquinoxaline-3-carbonitrile 1,4-dioxides new derivatives of quinoxaline and quinoxaline 1,4-dioxide were synthesized containing in the position 3 of the quinoxaline fragment 1,2,4-oxadiazole and tetrazole rings. The acylation of 2-amino-N'-hydroxyquinoxaline-3-carbox imidoamide 1,4-dioxide was investigated. Pleiades Publishing, Ltd., 2012.

Conversion of 3-Benzenesulfonyloxyalloxazine to 3-Hydroxyalloxazine by Acid Catalysed Hydrolysis

Mahajanshetti, C. S.,Kulkarni, S. U.

, p. 670 - 671 (2007/10/02)

Sodium 2,3-quinoxalinedicarbohydroxamate (1) is decomposed by water or even atmospheric moisture.Lossen rearrangement (LR) of anhydrous and decomposed 1 in the presence of benzenesulfonyl chloride and sodium acetate in THF has been reported. 3-Benzenesulf

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