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2-Fluoro-6-(hydroxymethyl)phenol is a chemical compound that features a phenol ring with a fluorine atom and a hydroxymethyl group at the 2 and 6 positions, respectively. It is known for its potential biological activities, such as antifungal and antimicrobial properties, and is utilized in various chemical and pharmaceutical applications.

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  • 446-58-2 Structure
  • Basic information

    1. Product Name: 2-Fluoro-6-(hydroxymethyl)phenol
    2. Synonyms: 2-Fluoro-6-(hydroxymethyl)phenol
    3. CAS NO:446-58-2
    4. Molecular Formula: C7H7FO2
    5. Molecular Weight: 142.1276832
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 446-58-2.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-Fluoro-6-(hydroxymethyl)phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Fluoro-6-(hydroxymethyl)phenol(446-58-2)
    11. EPA Substance Registry System: 2-Fluoro-6-(hydroxymethyl)phenol(446-58-2)
  • 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: 446-58-2(Hazardous Substances Data)

446-58-2 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Fluoro-6-(hydroxymethyl)phenol is used as a key building block in the synthesis of pharmaceuticals for its unique structural properties that can contribute to the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Fluoro-6-(hydroxymethyl)phenol is used as an intermediate, playing a crucial role in the formation of complex organic compounds.
Used as a Reagent in Chemical Reactions:
2-Fluoro-6-(hydroxymethyl)phenol serves as a reagent in various chemical reactions, facilitating specific transformations and syntheses.
Used in Antimicrobial Applications:
Leveraging its antimicrobial properties, 2-Fluoro-6-(hydroxymethyl)phenol is used as an antimicrobial agent, potentially contributing to the development of treatments for microbial infections.
Used in Antifungal Applications:
Due to its antifungal characteristics, 2-Fluoro-6-(hydroxymethyl)phenol is employed as an antifungal agent, which can be instrumental in creating solutions for fungal infections.

Check Digit Verification of cas no

The CAS Registry Mumber 446-58-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 446-58:
(5*4)+(4*4)+(3*6)+(2*5)+(1*8)=72
72 % 10 = 2
So 446-58-2 is a valid CAS Registry Number.

446-58-2SDS

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-Fluoro-6-(hydroxymethyl)phenol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:446-58-2 SDS

446-58-2Relevant articles and documents

Water-promoted ortho-selective monohydroxymethylation of phenols in the NaBO2 system

Li, Hui-Jing,Wu, Ying-Ying,Wu, Qin-Xi,Wang, Rui,Dai, Chun-Yang,Shen, Zhi-Lun,Xie, Cheng-Long,Wu, Yan-Chao

, p. 3100 - 3107 (2014/05/06)

Water-promoted ortho-selective monohydroxymethylation of phenols in the NaBO2 system generates salicyl alcohols in 65-97% yields. A remarkable rate-enhancement by water was observed, and NaBO2 appeared to serve the dual role of a suitable base and an efficient chelating reagent. This protocol possesses many advantages such as short reaction times, expanded substrate scope, and high mono- and regio-selectivities. The experimental results were explained by the calculations based on local ionisation energy minima, leading to a possible reaction mechanism.

MONOAMINE RE-UPTAKE INHIBITORS AND METHODS RELATING THERETO

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Page/Page column 29, (2010/11/25)

Monoamine re-uptake inhibitors and more specifically serotonin and noradrenaline re-uptake inhibitors are disclosed that have utility in the treatment of disorders of the central or peripheral nervous system in both men and women. The compounds of this invention have the structure: wherein R1, R2, R3, R4, R5, R6, m, n, W, X, Y, and Z are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts, esters and solvates thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for inhibiting monoamine re-uptake in a subject in need thereof.

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