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405137-17-9

4-Hydroxy-2-iodo-3-methoxypyridine is a chemical compound with the molecular formula C6H6INO2. It is a derivative of pyridine, which is a six-membered heterocyclic ring containing five carbon atoms and one nitrogen atom. The presence of a hydroxyl group and a methoxy group on the pyridine ring makes it a useful building block for the synthesis of various pharmaceutical and agrochemical products. The iodine substituent also imparts unique reactivity and properties to the molecule.
Used in Pharmaceutical Industry:
4-Hydroxy-2-iodo-3-methoxypyridine is used as a building block for the synthesis of various pharmaceutical products. Its unique structure and reactivity make it a promising candidate for the development of new drugs and therapeutics.
Used in Agrochemical Industry:
4-Hydroxy-2-iodo-3-methoxypyridine is used as a building block for the synthesis of various agrochemical products. Its unique structure and reactivity make it a valuable component in the development of new pesticides and other agrochemicals.
Used as a Reagent in Organic Synthesis:
4-Hydroxy-2-iodo-3-methoxypyridine is used as a reagent in organic synthesis. Its unique structure and reactivity make it a useful component in the synthesis of various organic compounds.
Used in the Production of Specialty Chemicals:
4-Hydroxy-2-iodo-3-methoxypyridine may be used in the production of specialty chemicals. Its unique structure and reactivity make it a valuable component in the development of specialty chemicals for various applications.
It is important to handle 4-Hydroxy-2-iodo-3-methoxypyridine with care, as it may pose health and environmental hazards if not used properly.

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  • 405137-17-9 Structure

  • Basic information

    1. Product Name: 4-Hyxdroxy-2-iodo-3-methoxypyridine
    2. Synonyms: 4-Hyxdroxy-2-iodo-3-methoxypyridine
    3. CAS NO:405137-17-9
    4. Molecular Formula: C6H6INO2
    5. Molecular Weight: 251.02
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 405137-17-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 462.5±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.974±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.08±0.10(Predicted)
    10. CAS DataBase Reference: 4-Hyxdroxy-2-iodo-3-methoxypyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Hyxdroxy-2-iodo-3-methoxypyridine(405137-17-9)
    12. EPA Substance Registry System: 4-Hyxdroxy-2-iodo-3-methoxypyridine(405137-17-9)

  • 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: 405137-17-9(Hazardous Substances Data)

405137-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 405137-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,1,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 405137-17:
(8*4)+(7*0)+(6*5)+(5*1)+(4*3)+(3*7)+(2*1)+(1*7)=109
109 % 10 = 9
So 405137-17-9 is a valid CAS Registry Number.

405137-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-3-methoxy-1H-pyridin-4-one

1.2 Other means of identification

Product number -
Other names 2-iodo-3-methoxypyridin-4-ol

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:405137-17-9 SDS

405137-17-9Relevant articles and documents

New syntheses of orelline and analogues via metalation and cross-coupling reactions

Mongin, Florence,Trécourt, Fran?ois,Mongin, Olivier,Quéguiner, Guy

, p. 309 - 314 (2002)

New total syntheses of orelline and some analogues are reported. The methodology involves metalation of 3-alkoxy-2-iodopyridines to afford 3,4-dialkoxy-2-iodopyridines, on which cross-coupling reactions are performed to reach the 2,2′-bipyridine skeleton of the alkaloid.

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