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3-Cyanopyridine-2-carboxylic acid is a chemical compound with the molecular formula C7H4N2O2, derived from pyridine and featuring both a carboxylic acid and a cyano group. This white crystalline solid is soluble in water and organic solvents, and it holds potential applications across various fields including medicine, agriculture, and chemical manufacturing.

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  • 53940-10-6 Structure
  • Basic information

    1. Product Name: 3-CYANOPYRIDINE-2-CARBOXYLIC ACID
    2. Synonyms: 3-CYANOPYRIDINE-2-CARBOXYLIC ACID;2-Pyridinecarboxylicacid,3-cyano-(9CI);3-cyano-2-Pyridinecarboxylic acid;2-Pyridinecarboxylic acid, 3-cyano-;3-Cyanopicolinic acid
    3. CAS NO:53940-10-6
    4. Molecular Formula: C7H4N2O2
    5. Molecular Weight: 148.12
    6. EINECS: 604-604-1
    7. Product Categories: CARBOXYLICACID
    8. Mol File: 53940-10-6.mol
  • Chemical Properties

    1. Melting Point: 175-176 °C
    2. Boiling Point: 371.6 °C at 760 mmHg
    3. Flash Point: 178.5 °C
    4. Appearance: /
    5. Density: 1.42 g/cm3
    6. Vapor Pressure: 3.52E-06mmHg at 25°C
    7. Refractive Index: 1.596
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 2.58±0.10(Predicted)
    11. CAS DataBase Reference: 3-CYANOPYRIDINE-2-CARBOXYLIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-CYANOPYRIDINE-2-CARBOXYLIC ACID(53940-10-6)
    13. EPA Substance Registry System: 3-CYANOPYRIDINE-2-CARBOXYLIC ACID(53940-10-6)
  • 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: 53940-10-6(Hazardous Substances Data)

53940-10-6 Usage

Uses

Used in Pharmaceutical Industry:
3-Cyanopyridine-2-carboxylic acid is used as a building block for the synthesis of various drugs and pharmaceutical intermediates, contributing to the development of new therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 3-Cyanopyridine-2-carboxylic acid is utilized for the production of compounds that aid in crop protection and enhancement of agricultural yields.
Used in Dye Manufacturing:
3-Cyanopyridine-2-carboxylic acid is employed as a key intermediate in the synthesis of dyes, contributing to the coloration and quality of various products.
Used in Organic Compounds Synthesis:
3-Cyanopyridine-2-carboxylic acid serves as a versatile intermediate in the synthesis of other organic compounds, expanding its utility in the chemical manufacturing sector.

Check Digit Verification of cas no

The CAS Registry Mumber 53940-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,4 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53940-10:
(7*5)+(6*3)+(5*9)+(4*4)+(3*0)+(2*1)+(1*0)=116
116 % 10 = 6
So 53940-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4N2O2/c8-4-5-2-1-3-9-6(5)7(10)11/h1-3H,(H,10,11)

53940-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyanopyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-cyano-pyridine-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:53940-10-6 SDS

53940-10-6Relevant articles and documents

PREPARATION AND STRUCTURAL ASSIGNMENTS OF SOME ISOMERIC 2,3-DISUBSTITUTED PYRIDINES

Spiessens, Luc I. M.,Anteunis, Marc J. O.

, p. 205 - 232 (2007/10/02)

The preparation of several isomeric 2,3-disubstituted pyridine compounds are described and their spectroscopical data given.IR and NMR spectra of quinolinimide, reported by Distefano et al., are contradicted.The electron impact mass spectra are found to be useful in the differentiation between positional isomers.

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