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69411-67-2

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69411-67-2 Usage

Chemical Properties

colorless to light yellow liqui

Uses

2-Fluoro-4-nitrobenzotrifluoride is a reagent in the synthesis of benzylamine and benzylsulfone antagonists of urotensin receptor (UT).

Check Digit Verification of cas no

The CAS Registry Mumber 69411-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69411-67:
(7*6)+(6*9)+(5*4)+(4*1)+(3*1)+(2*6)+(1*7)=142
142 % 10 = 2
So 69411-67-2 is a valid CAS Registry Number.
InChI:InChI=1S/C7H3F4NO2/c8-6-3-4(12(13)14)1-2-5(6)7(9,10)11/h1-3H

69411-67-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H64300)  2-Fluoro-4-nitrobenzotrifluoride, 98%   

  • 69411-67-2

  • 250mg

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64300)  2-Fluoro-4-nitrobenzotrifluoride, 98%   

  • 69411-67-2

  • 1g

  • 588.0CNY

  • Detail
  • Alfa Aesar

  • (H64300)  2-Fluoro-4-nitrobenzotrifluoride, 98%   

  • 69411-67-2

  • 5g

  • 2352.0CNY

  • Detail

69411-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-4-nitro-1-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 2-fluoro-4-nitro-1-(trifluoromethyl)benzene

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:69411-67-2 SDS

69411-67-2Relevant articles and documents

Deoxofluorination of (Hetero)aromatic Acids

Alekseenko, Anatoliy N.,Bugera, Maksym Ya.,Gerus, Igor I.,Kiriakov, Oleksandr,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Pustovit, Yurii,Razhyk, Bohdan,Semenov, Sergey,Starova, Viktoriia S.,Tananaiko, Oksana Yu.,Tarasenko, Karen,Tolmachev, Andrei A.,Trofymchuk, Serhii,Zaporozhets, Olga A.

, p. 3110 - 3124 (2020/03/23)

Diverse trifluoromethyl-substituted compounds were synthesized by deoxofluorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride. The obtained products were used as starting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building blocks for medicinal chemistry and agrochemistry.

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