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174469-05-7

(2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is a heterocyclic chemical compound featuring a fused bicyclic structure that includes a furo[2,3-c]pyridine ring system and a hydroxymethyl group attached to the pyridine ring. This unique structure, along with its functional groups, positions it as a valuable building block in organic synthesis and medicinal chemistry research. Its potential in drug discovery and development underscores its significance in the fields of organic chemistry and medicinal chemistry.

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  • 174469-05-7 Structure

  • Basic information

    1. Product Name: (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol
    2. Synonyms: Furo[2,3-c]pyridine-3-methanol, 2,3-dihydro-
    3. CAS NO:174469-05-7
    4. Molecular Formula: C8H9NO2
    5. Molecular Weight: 151.16256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174469-05-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(174469-05-7)
    11. EPA Substance Registry System: (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(174469-05-7)

  • 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: 174469-05-7(Hazardous Substances Data)

174469-05-7 Usage

Uses

Used in Organic Synthesis:
(2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol serves as a key intermediate in various organic synthesis processes due to its reactive functional groups and heterocyclic nature, which can be further modified to produce a range of chemical products.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is utilized as a starting material for the development of potentially bioactive molecules. Its unique structure allows for the design and synthesis of new compounds with therapeutic potential.
Used in Drug Discovery and Development:
(2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is an important target for drug discovery and development efforts. Its incorporation into pharmaceutical drugs can lead to the creation of novel therapeutic agents with improved efficacy and selectivity for various medical conditions.
Used in Pharmaceutical Industry:
(2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is used as a building block for the synthesis of pharmaceutical drugs, contributing to the development of new medications with innovative mechanisms of action and improved patient outcomes.
Used in Chemical Research:
In academic and industrial chemical research settings, (2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is employed as a subject of study to explore its chemical properties, reactivity, and potential applications in creating new materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 174469-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 174469-05:
(8*1)+(7*7)+(6*4)+(5*4)+(4*6)+(3*9)+(2*0)+(1*5)=157
157 % 10 = 7
So 174469-05-7 is a valid CAS Registry Number.

174469-05-7Relevant articles and documents

SYNTHESIS OF N-SUBSTITUTED 3-AMINOMETHYL-2,3-DIHYDROFUROPYRIDINES, POTENT SEROTONINERGIC LIGANDS

Joseph, Benoit,Benarab, Abdelhakim,Guillaumet, Gerald

, p. 2769 - 2776 (2007/10/03)

Regioselective lithiation of 2-chloro-3-oxiranylmethoxypyridine, followed by intramolecular epoxide ring-opening reaction provided (7-chloro-2,3-dihydrofuropyridin-3-yl>methanol (1).Multistep synthesis from 1 gave a variety of N-substituted 3-amino

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