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CAS

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2-Fluoro-5-(trifluoromethyl)phenol is an organic fluorinated building block, characterized by its clear colorless to orange liquid appearance. It is a compound that holds potential in various applications due to its unique chemical properties.

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  • 141483-15-0 Structure
  • Basic information

    1. Product Name: 2-Fluoro-5-(trifluoromethyl)phenol
    2. Synonyms: 2-FLUORO-5-(TRIFLUOROMETHYL)PHENOL98+% (GC);2-Fluoro-5-(trifluor;2-Fluoro-5-(trifuoroMethyl)phenol;5-FLUORO-ALPHA-ALPHA-ALPHA-TRIFLUORO-M-CRESOL;4-FLUORO-3-HYDROXYBENZOTRIFLUORIDE;2-FLUORO-5-(TRIFLUOROMETHYL)PHENOL;alpha,alpha,alpha,6-Tetrafluoro-m-cresol;à,à,à,6-tetrafluoro-m-cresol
    3. CAS NO:141483-15-0
    4. Molecular Formula: C7H4F4O
    5. Molecular Weight: 180.1
    6. EINECS: N/A
    7. Product Categories: Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Organic Building Blocks;Oxygen Compounds;Phenols;Fluorine series
    8. Mol File: 141483-15-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 146 °C(lit.)
    3. Flash Point: 135 °F
    4. Appearance: Clear colorless to orange/Liquid
    5. Density: 1.436 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 1.59mmHg at 25°C
    7. Refractive Index: n20/D 1.439(lit.)
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. PKA: 7.70±0.10(Predicted)
    11. BRN: 8392138
    12. CAS DataBase Reference: 2-Fluoro-5-(trifluoromethyl)phenol(CAS DataBase Reference)
    13. NIST Chemistry Reference: 2-Fluoro-5-(trifluoromethyl)phenol(141483-15-0)
    14. EPA Substance Registry System: 2-Fluoro-5-(trifluoromethyl)phenol(141483-15-0)
  • Safety Data

    1. Hazard Codes: Xn,T
    2. Statements: 20/21/22-36/37/38
    3. Safety Statements: 26-36
    4. RIDADR: UN 1993 3/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: 3
    8. PackingGroup: III
    9. Hazardous Substances Data: 141483-15-0(Hazardous Substances Data)

141483-15-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-5-(trifluoromethyl)phenol is used as an intermediate for the synthesis of various pharmaceutical compounds. Its fluorinated structure contributes to the development of new drugs with improved pharmacological properties, such as enhanced bioavailability and selectivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Fluoro-5-(trifluoromethyl)phenol serves as a key building block for creating a range of fluorinated organic compounds. These compounds find applications in various industries, including agrochemicals, materials science, and specialty chemicals.
Used in Material Science:
2-Fluoro-5-(trifluoromethyl)phenol is used as a component in the development of advanced materials with specific properties, such as high thermal stability, chemical resistance, and low surface energy. These materials can be utilized in coatings, adhesives, and other industrial applications.
Used in Agrochemicals:
In the agrochemical industry, 2-Fluoro-5-(trifluoromethyl)phenol is used as a starting material for the synthesis of novel pesticides and herbicides. Its fluorinated nature can lead to the creation of more effective and environmentally friendly agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 141483-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141483-15:
(8*1)+(7*4)+(6*1)+(5*4)+(4*8)+(3*3)+(2*1)+(1*5)=110
110 % 10 = 0
So 141483-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F4O/c8-5-2-1-4(3-6(5)12)7(9,10)11/h1-3,12H

141483-15-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (B20004)  2-Fluoro-5-(trifluoromethyl)phenol, 97%   

  • 141483-15-0

  • 1g

  • 377.0CNY

  • Detail
  • Alfa Aesar

  • (B20004)  2-Fluoro-5-(trifluoromethyl)phenol, 97%   

  • 141483-15-0

  • 5g

  • 1309.0CNY

  • Detail
  • Aldrich

  • (436127)  2-Fluoro-5-(trifluoromethyl)phenol  97%

  • 141483-15-0

  • 436127-5G

  • 1,009.71CNY

  • Detail

141483-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-5-(trifluoromethyl)phenol

1.2 Other means of identification

Product number -
Other names 2-FLUORO-5-(TRIFLUOROMETHYL)PHENOL (GC)

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:141483-15-0 SDS

141483-15-0Relevant articles and documents

Pd-Catalyzed debenzylation and deallylation of ethers and esters with sodium hydride

Mao, Yujian,Liu, Ye,Hu, Yanwei,Wang, Liang,Zhang, Shilei,Wang, Wei

, p. 3016 - 3020 (2018/04/14)

Herein we demonstrate simply that the addition of Pd(OAc)2 as a promotor switches the reactivity of a commonly used base NaH to a nucleophilic reductant. The reactivity is engineered into a palladium-catalyzed reductive debenzylation and deallylation of aryl ethers and esters. This operationally simple, mild protocol displays a broad substrate scope and a broad spectrum of functional group tolerance (>50 examples) and high chemoselectivity toward aryl ethers over aliphatic structures. Moreover, the dual reactivity of NaH as a base and a reductant is demonstrated in efficient synthetic elaboration.

Synthesis of 2 - fluoro phenol compounds

-

, (2017/04/21)

The present invention provides a method for synthetizing a 2-fluoro phenol compound shown in a formula IV. The phenol compound shown in the formula I is prepared into a 2-pyridine oxygroup arene compound shown in a formula II through an Ullmann reaction, the 2-pyridine oxygroup arene compound shown in the formula II is mixed with a palladium catalyst, a fluorinating reagent, an additive and an organic solvent, the mixture is stirred under the temperature of 30-160 DEG C to perform a fluorination reaction to obtain an ortho-position fluoridated 2-pyridine oxygroup arene compound shown in a formula III, and the ortho-position fluoridated 2-pyridine oxygroup arene compound shown in the formula III is prepared into the 2-fluoro phenol compound shown in the formula IV through the action of alkali. The method provided by the present invention has the advantages of mild reaction conditions, simplicity in operations, good substrate adaptability, high fluorination selectivity and the like. The 2-fluoro phenol compound is shown in the figure below.

6-(Nonsubstituted or substituted) phenoxy picolinic acids, process of preparing the same, and agricultural/horticultural germicides containing the same

-

, (2008/06/13)

An agricultural or horticultural fungicide containing 6-(unsubstituted or substituted) phenoxy picolinic acid represented by the general formula (I), as an effective ingredient. wherein R is a halogen atom, a C1to C4alkyl group, a C1to C4haloalkyl group, a C1to C4alkoxy group, a C1to C4haloalkoxy group, a C1to C4alkylthio group, a C1to C4alkylamino group, a di(C1to C4alkyl)amino group or a C7to C8aralkyl(C1to C4alkyl)amino group; n2is an integer of 0 to 3; Y is a C1to C4alkyl group, a C1to C4haloalkyl group, a C1to C4alkoxy group, a C1to C4haloalkoxy group, a C1to C4alkylthio group, a C1to C4haloalkylthio group or a halogen atom; and m is an integer of 0 to 5, and when m and n2are not less than 2, Rs and Ys may be the same or different, respectively. The compound is useful as an effective ingredient of agricultural or horticultural fungicides.

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