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2-Fluoro-4-(trifluoroMethoxy)aniline, 97% is an aromatic amine compound with a purity of 97%. It contains fluorine and trifluoromethoxy functional groups, making it a versatile compound for various applications.
Used in Pharmaceutical Industry:
2-Fluoro-4-(trifluoroMethoxy)aniline, 97% is used as a building block for the synthesis of various organic compounds in the pharmaceutical industry. Its unique functional groups allow for the development of new drugs with improved properties.
Used in Agrochemical Industry:
2-Fluoro-4-(trifluoroMethoxy)aniline, 97% is used as an intermediate in the manufacturing of agrochemicals. Its presence in these compounds can enhance their effectiveness and selectivity in pest control.
Used in Electronic Materials Industry:
2-Fluoro-4-(trifluoroMethoxy)aniline, 97% is used in the development of electronic materials due to its unique properties. It can contribute to the creation of advanced materials for use in electronic devices and components.
Used in Dyes and Pigments Industry:
2-Fluoro-4-(trifluoroMethoxy)aniline, 97% is used as an intermediate in the manufacturing of dyes and pigments. Its incorporation into these compounds can result in improved color properties and stability.

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  • 123572-58-7 Structure
  • Basic information

    1. Product Name: 2-Fluoro-4-(trifluoroMethoxy)aniline, 97%
    2. Synonyms: 2-Fluoro-4-(trifluoroMethoxy)aniline, 97%
    3. CAS NO:123572-58-7
    4. Molecular Formula: C7H5F4NO
    5. Molecular Weight: 195.1143128
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123572-58-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 161.4±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.431±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.35±0.10(Predicted)
    10. CAS DataBase Reference: 2-Fluoro-4-(trifluoroMethoxy)aniline, 97%(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Fluoro-4-(trifluoroMethoxy)aniline, 97%(123572-58-7)
    12. EPA Substance Registry System: 2-Fluoro-4-(trifluoroMethoxy)aniline, 97%(123572-58-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: 6.1
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 123572-58-7(Hazardous Substances Data)

123572-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123572-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,7 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123572-58:
(8*1)+(7*2)+(6*3)+(5*5)+(4*7)+(3*2)+(2*5)+(1*8)=117
117 % 10 = 7
So 123572-58-7 is a valid CAS Registry Number.

123572-58-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H33844)  2-Fluoro-4-(trifluoromethoxy)aniline, 97%   

  • 123572-58-7

  • 250mg

  • 605.0CNY

  • Detail
  • Alfa Aesar

  • (H33844)  2-Fluoro-4-(trifluoromethoxy)aniline, 97%   

  • 123572-58-7

  • 1g

  • 2012.0CNY

  • Detail

123572-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-4-(trifluoromethoxy)aniline

1.2 Other means of identification

Product number -
Other names 2-FLUORO-4-(TRIFLUOROMETHOXY)BENZENAMINE

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:123572-58-7 SDS

123572-58-7Relevant articles and documents

6-OXO-1,6-DIHYDROPYRIDAZINE DERIVATIVE, PREPARATION METHOD THEREFOR AND MEDICAL USE THEREOF

-

, (2021/11/14)

A 6-oxo-1,6-dihydropyridazine derivative, a preparation method therefor and medical use thereof, in particular, a 6-oxo-1,6-dihydropyridazine derivative represented by general formula (I), a preparation method therefor, and a pharmaceutical composition containing the derivative, and use thereof as a NaV inhibitor and use thereof in the preparation of a drug for the treatment and/or prevention of pain and pain-related diseases. Each substituent in general formula (I) is the same as defined in the description.

Anion ligand promoted selective C-F bond reductive elimination enables C(sp2)-H fluorination

Mao, Yang-Jie,Luo, Gen,Hao, Hong-Yan,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian

supporting information, p. 14458 - 14461 (2019/12/09)

A detailed mechanism study on the anion ligand promoted selective C-H bond fluorination is reported. The role of the anion ligand has been clarified by experimental evidence and DFT calculations. Moreover, the nitrate promoted C-F bond reductive elimination enabled a selective C-H bond fluorination of various symmetric and asymmetric azobenzenes to access diverse o-fluoroanilines.

KAPPA OPIOID RECEPTOR ANTAGONISTS AND PRODUCTS AND METHODS RELATED THERETO

-

Page/Page column 191; 195; 198, (2018/10/19)

Compounds are provided that antagonize the kappa-opioid receptor (KOR) and products containing such compounds, as well as to methods of their use and synthesis. Such compounds have the structure of Formula (I), or a pharmaceutically acceptable isomer, racemate, hydrate, solvate, isotope or salt thereof: (I) wherein X, Y, R1, R2, R4, R5 R6, R7, R8 and R11 are as defined herein.

Pyridazinone compounds

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Page/Page column 77, (2010/08/08)

The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I0): wherein R1 represents a substituent, R2 represents a hydrogen atom, or a substituent, R3 represents a hydrogen atom, or a substituent, Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.

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