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174469-04-6

(7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is a chemical compound with the molecular formula C8H8ClNO2. It is a furo[2,3-c]pyridine derivative characterized by the presence of a chlorine atom and a hydroxymethyl group attached to the pyridine ring. (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol possesses potential pharmacological properties, making it a promising candidate for the development of new pharmaceuticals or as a research reagent in the field of medicinal chemistry and drug discovery.

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  • 174469-04-6 Structure

  • Basic information

    1. Product Name: (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol
    2. Synonyms: 7-chloro-2,3-dihydro-Furo[2,3-c]pyridine-3-methanol
    3. CAS NO:174469-04-6
    4. Molecular Formula: C8H8ClNO2
    5. Molecular Weight: 185.60762
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174469-04-6.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: (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(174469-04-6)
    11. EPA Substance Registry System: (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol(174469-04-6)

  • 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: 174469-04-6(Hazardous Substances Data)

174469-04-6 Usage

Uses

Used in Pharmaceutical Development:
(7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups contribute to its potential as a building block for the development of novel therapeutic agents.
Used in Medicinal Chemistry Research:
As a research reagent, (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol is utilized in the exploration of its biological activity and potential applications in medicinal chemistry. Its unique structure allows researchers to investigate its interactions with biological targets and evaluate its efficacy in treating specific diseases or conditions.
Used in Drug Discovery:
(7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol serves as a valuable compound in drug discovery processes. Its unique structural features and potential pharmacological properties make it an interesting target for further study, with the aim of identifying new drug candidates and advancing the development of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 174469-04-6 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 174469-04:
(8*1)+(7*7)+(6*4)+(5*4)+(4*6)+(3*9)+(2*0)+(1*4)=156
156 % 10 = 6
So 174469-04-6 is a valid CAS Registry Number.

174469-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-chloro-2,3-dihydrofuro[2,3-c]pyridin-3-yl)methanol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:174469-04-6 SDS

174469-04-6Relevant 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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