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3-Pyridinol,4-methoxy-(9CI) is a chemical compound with the molecular formula C6H7NO2, belonging to the pyridine derivative family. It features a methoxy group attached to the fourth carbon atom, which endows it with unique chemical properties and potential applications across various industries.

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  • 153199-54-3 Structure
  • Basic information

    1. Product Name: 3-Pyridinol,4-methoxy-(9CI)
    2. Synonyms: 3-Pyridinol,4-methoxy-(9CI);3-Hydroxy-4-methoxypyridine;4-Methoxy-3-hydroxypyridine;4-methoxy-3-Pyridinol
    3. CAS NO:153199-54-3
    4. Molecular Formula: C6H7NO2
    5. Molecular Weight: 125.13
    6. EINECS: 604-604-1
    7. Product Categories: PYRIDINE
    8. Mol File: 153199-54-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 326.104 °C at 760 mmHg
    3. Flash Point: 151.023 °C
    4. Appearance: /
    5. Density: 1.191 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.539
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. PKA: 9.44±0.18(Predicted)
    11. CAS DataBase Reference: 3-Pyridinol,4-methoxy-(9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-Pyridinol,4-methoxy-(9CI)(153199-54-3)
    13. EPA Substance Registry System: 3-Pyridinol,4-methoxy-(9CI)(153199-54-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 153199-54-3(Hazardous Substances Data)

153199-54-3 Usage

Uses

Used in Pharmaceutical Industry:
3-Pyridinol,4-methoxy-(9CI) is used as a building block for the synthesis of various drugs and pharmaceuticals. Its unique structure allows it to be a key component in the development of new medications, contributing to the advancement of healthcare.
Used in Neurological Disorders Treatment:
3-Pyridinol,4-methoxy-(9CI) has been studied for its potential use in the treatment of neurological disorders. Its specific chemical properties may offer therapeutic benefits in managing or alleviating symptoms associated with such conditions, thereby improving patient outcomes.
Used in Agrochemicals Synthesis:
3-Pyridinol,4-methoxy-(9CI) also serves as a precursor in the synthesis of agrochemicals. Its role in creating effective compounds for agricultural applications can contribute to enhanced crop protection and yield, supporting global food security and agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 153199-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,9 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153199-54:
(8*1)+(7*5)+(6*3)+(5*1)+(4*9)+(3*9)+(2*5)+(1*4)=143
143 % 10 = 3
So 153199-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c1-9-6-2-3-7-4-5(6)8/h2-4,8H,1H3

153199-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxypyridin-3-ol

1.2 Other means of identification

Product number -
Other names 4-methoxypyridin-3-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:153199-54-3 SDS

153199-54-3Relevant articles and documents

A concise approach towards the synthesis of WS75624 a and WS75624 B via the cross-metathesis of vinyl-functionalized thiazoles

Dash, Jyotirmayee,Melillo, Bruno,Arseniyadis, Stellios,Cossy, Janine

scheme or table, p. 2246 - 2249 (2011/05/05)

Synthetic approach towards precursors of WS75624 A and WS75624 B, two potent endothelin converting enzyme (ECE) inhibitors and potential antihypertensive agents, is reported featuring a key cross-metathesis between a vinyl-functionalized thiazole and a terminal olefin. As the two natural products only differ by the nature of their hydroxyalkyl side-chain, our convergent strategy enable the synthesis of key intermediates of both molecules in a limited amount of steps.

Total synthesis of the antifungal dilactones UK-2A and UK-3A: The determination of their relative and absolute configurations, analog synthesis and antifungal activities

Shimano, Masanao,Kamei, Noriyuki,Shibata, Tetsuo,Inoguchi, Kiyoshi,Itoh, Nobuko,Ikari, Takashi,Senda, Hisato

, p. 12745 - 12774 (2007/10/03)

The synthesis of the antifungal dilactones, UK-2A and UK-3A, is described. In addition to providing a workable synthetic route to these potent antifungal antibiotics, this has allowed us to determine the assignment of the relative and absolute configurations in the nine-membered ring. Furthermore, UK-2A analogs were also synthesized and evaluated their antifungal activities and cytotoxic activities along with UK-2A, (2R, 3R, 4S, 7R)-UK-2A, UK-3A, (2R, 3R, 4S, 7R)-UK-3A, and antimycin A. The structural requirements for the selective cytotoxicity against yeasts and filamentous fungi will also be suggested.

New Synthesis of Orelline by Metalation of Methoxypyridines

Trecourt, Francois,Mallet, Marc,Mongin, Olivier,Gervais, Bruno,Queguiner, Guy

, p. 8373 - 8380 (2007/10/02)

A new total synthesis in five steps of alkaloid Orelline is reported.The methodology involves metalation of methoxypyridines to afford 2-halo-3,4-dimethoxypyridine on which an homocoupling reaction is performed to build the 2,2'-bipyridyl structure of the

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