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151868-17-6

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151868-17-6 Usage

General Description

2-Fluoro-3-(trifluoromethyl)anisole is a type of chemical compound, belonging to the classification of aromatic compounds, particularly anisoles. Anisoles consist of a methoxy group bonded to a phenyl group. This specific compound has a fluorine atom and a trifluoromethyl group further attached to its benzene ring. Characteristics of this chemical, such as its exact molecular structure, weight, boiling point, melting point, and other physical properties could vary. Its particular uses or applications can differ, but generally, these types of compounds can be used within various chemical reactions as intermediate products or directly in the manufacturing of certain types of chemical substances, drugs, pesticides or other industrial chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 151868-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,8,6 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151868-17:
(8*1)+(7*5)+(6*1)+(5*8)+(4*6)+(3*8)+(2*1)+(1*7)=146
146 % 10 = 6
So 151868-17-6 is a valid CAS Registry Number.

151868-17-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H26642)  2-Fluoro-3-(trifluoromethyl)anisole, 97%   

  • 151868-17-6

  • 1g

  • 640.0CNY

  • Detail
  • Alfa Aesar

  • (H26642)  2-Fluoro-3-(trifluoromethyl)anisole, 97%   

  • 151868-17-6

  • 5g

  • 2131.0CNY

  • Detail

151868-17-6SDS

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 2-fluoro-1-methoxy-3-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 2-Fluoro-3-(trifluoromethyl)anisole

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:151868-17-6 SDS

151868-17-6Relevant articles and documents

Preparation of Indolenines via Nucleophilic Aromatic Substitution

Huber, Florian,Roesslein, Joel,Gademann, Karl

supporting information, p. 2560 - 2564 (2019/03/19)

An unusual aromatic substitution to access indolenines is described. 2-(2-Methoxyphenyl)acetonitrile derivatives are reacted with various alkyl and aryl Li reagents to furnish the corresponding indolenine products, constituents of natural products, and cyanine dyes such as indocyanine green. This new method was used to synthesize 41 indolenines with large functional group tolerance, and selected examples were further converted to the corresponding indolenine dyes. Key experiments provide insight into the mechanism of this nucleophilic aromatic substitution.

Process for selectively ortho-fluorinating substituted aromatic compounds

-

, (2008/06/13)

The invention describes a process for selectively preparing ortho-fluorinated substituted aromatic compounds wherein an aromatic compound containing a substituent capable of directing ortho metalation is contacted with a metalating reagent under reaction conditions sufficient to form an ortho-metalated substituted aromatic compound. The ortho-metalated substituted aromatic compound is reacted with an electrophilic fluorinating reagent under reaction conditions sufficient to form the desired ortho-fluorinated substituted aromatic compound which is then recovered from the reaction mixture. The process which utilizes a metalation intermediate prior to effecting the electrophilic fluorination step overcomes problems associated with prior art electrophilic fluorination processes which do not proceed through a regiospecifically controlled intermediate.

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