60611-24-7 Usage
Description
2-Fluoro-6-(trifluoromethyl)benzaldehyde is an organic compound characterized by the presence of a fluorine atom at the 2nd position and a trifluoromethyl group at the 6th position on a benzene ring. It is an important intermediate in the synthesis of various organic compounds and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
2-Fluoro-6-(trifluoromethyl)benzaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals, including diaryl ethers, which are known for their diverse biological activities and potential therapeutic applications.
Used in Chemical Synthesis:
2-Fluoro-6-(trifluoromethyl)benzaldehyde is used as a starting material for the synthesis of 2-(3,5-dimethoxyphenoxy)-6-(trifluoromethyl)-benzonitrile, a compound with potential applications in the development of new drugs and agrochemicals.
Used in Organic Chemistry:
2-Fluoro-6-(trifluoromethyl)benzaldehyde is employed as a precursor in the synthesis of substituted benzo[b]thiophene-2-carboxylates, which are valuable building blocks in organic chemistry and can be used to construct a variety of complex organic molecules with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 60611-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,1 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60611-24:
(7*6)+(6*0)+(5*6)+(4*1)+(3*1)+(2*2)+(1*4)=87
87 % 10 = 7
So 60611-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F4O/c9-7-3-1-2-6(5(7)4-13)8(10,11)12/h1-4H
60611-24-7Relevant articles and documents
Method for preparing 2-fluoro-6-trifluoromethylbenzaldehyde by using continuous flow reaction device
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Paragraph 0025-0048, (2020/03/13)
The embodiment of the invention discloses a method for preparing 2-fluoro-6-trifluoromethylbenzaldehyde by using a continuous flow reaction device, and belongs to the technical field of pharmaceuticaland chemical synthesis. The method includes: reacting a
PROCESSES TO PRODUCE ELAGOLIX
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Page/Page column 10, (2019/06/23)
The present invention relates to a scalable process for the making of elagolix, its salts and the process of intermediate compounds.
Regioselective formylation of 1,3-disubstituted benzenes through in situ lithiation
Wang, Le,Wang, Yan,Guo, Fangxu,Zheng, Yue,Bhadury, Pinaki S.,Sun, Zhihua
supporting information, p. 6053 - 6056 (2013/10/22)
A facile method of regioselective formylation of disubstituted benzene via in situ deprotonation/metalation using n-BuLi/TMEDA/DIPA has been developed. Effect of different electron withdrawing and electron donating substituents in 1,3-interrelated aromatic system was studied; the metalation mostly occurred at the 2-position to afford the desired products in high yields.