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2-Hydroxy-6-nitro-quinoline-3-carboxylic acid, an organic compound with the molecular formula C10H6N2O5, features a quinoline ring with a hydroxy group at position 2, a nitro group at position 6, and a carboxylic acid group at position 3. Its unique structure and functional groups render it a valuable building block for the production of bioactive molecules and pharmaceuticals.

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  • 85870-49-1 Structure
  • Basic information

    1. Product Name: 2-HYDROXY-6-NITRO-QUINOLINE-3-CARBOXYLIC ACID
    2. Synonyms: 3-Quinolinecarboxylic acid, 1,2-dihydro-6-nitro-2-oxo-;1,2-Dihydro-6-nitro-2-oxo-3-quinolinecarboxylic acid
    3. CAS NO:85870-49-1
    4. Molecular Formula: C10H6N2O5
    5. Molecular Weight: 234.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85870-49-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 527.74°C at 760 mmHg
    3. Flash Point: 272.968°C
    4. Appearance: /
    5. Density: 1.624g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.675
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-HYDROXY-6-NITRO-QUINOLINE-3-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-HYDROXY-6-NITRO-QUINOLINE-3-CARBOXYLIC ACID(85870-49-1)
    12. EPA Substance Registry System: 2-HYDROXY-6-NITRO-QUINOLINE-3-CARBOXYLIC ACID(85870-49-1)
  • 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: 85870-49-1(Hazardous Substances Data)

85870-49-1 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Hydroxy-6-nitro-quinoline-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its presence in the molecular structure allows for the development of drugs with specific therapeutic properties.
Used in Organic Chemistry as a Reagent:
In the field of organic chemistry, 2-Hydroxy-6-nitro-quinoline-3-carboxylic acid serves as a reagent in various chemical reactions. Its functional groups enable it to participate in a range of organic transformations, facilitating the synthesis of complex organic molecules.
Used in the Production of Bioactive Molecules:
Due to its unique structure, 2-Hydroxy-6-nitro-quinoline-3-carboxylic acid is utilized in the creation of bioactive molecules. These molecules have potential applications in medicine, agriculture, and other industries where bioactivity is crucial for their function.

Check Digit Verification of cas no

The CAS Registry Mumber 85870-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85870-49:
(7*8)+(6*5)+(5*8)+(4*7)+(3*0)+(2*4)+(1*9)=171
171 % 10 = 1
So 85870-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N2O5/c13-9-7(10(14)15)4-5-3-6(12(16)17)1-2-8(5)11-9/h1-4H,(H,11,13)(H,14,15)

85870-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-2-oxo-1H-quinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-hydroxy-6-nitroquinoline-3-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:85870-49-1 SDS

85870-49-1Relevant articles and documents

Identification of Quinoline Nitration Products by NOE

Hutt, Marland P.,MacKellar, Forrest A.

, p. 349 - 352 (2007/10/02)

The structures of the products from the nitration of 2- and 4-oxodihydroquinolines were assigned based on Nuclear Overhauser Effects of their nmr spectra and confirmed by unambiguous synthesis.

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