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2-Cyano-5-iodopyridine is a pyridine derivative with the molecular formula C6H3IN2, featuring a cyano group and an iodine atom attached to the 2 and 5 positions of the pyridine ring, respectively. This chemical compound serves as a versatile building block in various fields due to its unique structural properties.

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  • 41960-47-8 Structure
  • Basic information

    1. Product Name: 2-CYANO-5-IODOPYRIDINE
    2. Synonyms: 2-CYANO-5-IODOPYRIDINE;5-iodopyridine-2-carbonitrile;5-iodo-2-Pyridinecarbonitrile
    3. CAS NO:41960-47-8
    4. Molecular Formula: C6H3IN2
    5. Molecular Weight: 230.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41960-47-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 314.3 °C at 760 mmHg
    3. Flash Point: 143.9 °C
    4. Appearance: /
    5. Density: 2.04 g/cm3
    6. Vapor Pressure: 0.000469mmHg at 25°C
    7. Refractive Index: 1.669
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: -2.34±0.10(Predicted)
    11. CAS DataBase Reference: 2-CYANO-5-IODOPYRIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-CYANO-5-IODOPYRIDINE(41960-47-8)
    13. EPA Substance Registry System: 2-CYANO-5-IODOPYRIDINE(41960-47-8)
  • 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: 41960-47-8(Hazardous Substances Data)

41960-47-8 Usage

Uses

Used in Organic Synthesis:
2-Cyano-5-iodopyridine is used as a versatile building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for the synthesis of a wide range of compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyano-5-iodopyridine is used as a key intermediate in the synthesis of biologically active molecules. Its presence in the molecular structure can contribute to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
2-Cyano-5-iodopyridine is employed as a reagent in the production of heterocyclic compounds, which are often found in agrochemicals. These heterocyclic compounds can be used as pesticides, herbicides, or other agricultural chemicals to protect crops and enhance agricultural productivity.
Used in Material Science:
2-Cyano-5-iodopyridine has been studied for its potential applications in material science. Its unique structural properties may contribute to the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics.
Used in Medicinal Chemistry:
In medicinal chemistry, 2-Cyano-5-iodopyridine is used as a precursor in the synthesis of biologically active molecules. Its presence in the molecular structure can enhance the pharmacological properties of the resulting compounds, leading to the development of more effective drugs for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 41960-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,6 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41960-47:
(7*4)+(6*1)+(5*9)+(4*6)+(3*0)+(2*4)+(1*7)=118
118 % 10 = 8
So 41960-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3IN2/c7-5-1-2-6(3-8)9-4-5/h1-2,4H

41960-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodopyridine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-iodo-pyridine-2-carbonitrile

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:41960-47-8 SDS

41960-47-8Relevant articles and documents

DERIVATIVES OF 6,7-DIHYDRO-5H-IMIDAZO[1,2-α]IMIDAZOLE-3- CARBOXYLIC ACID AMIDES

-

Page/Page column 112-113, (2009/07/03)

Derivatives of 6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-carboxylic acid amide exhibit good inhibitory effect upon the interaction of CAMs and Leukointegrins and are thus useful in the treatment of inflammatory disease.

A simple Cu-catalyzed coupling approach to substituted 3-pyridinol and 5-pyrimidinol antioxidants

Nara, Susheel J.,Jha, Mukund,Brinkhorst, Johan,Zemanek, Tony J.,Pratt, Derek A.

supporting information; experimental part, p. 9326 - 9333 (2009/04/06)

(Chemical Equation Presented) A convenient approach to 3-pyridinols and 5-pyrimidinols via a two-step Cu-catalyzed benzyloxylation/catalytic hydrogenation sequence is presented. The corresponding 3-pyridinamines and 5-pyrimidinamines can be prepared in an analogous sequence utilizing benzylamine in lieu of benzyl alcohol. The radical-scavenging ability of these derivatives are preliminarily explored and reveal that the increased acidities of the pyridinols and pyrimidinols render them susceptible to more significant kinetic solvent effects when compared to phenols.

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