106312-36-1 Usage
Description
4-Methoxy-2-(trifluoromethyl)benzaldehyde is an organic chemical compound that features aromatic aldehyde and aromatic ether functionalities. It is distinguished by a benzene ring with a trifluoromethyl group, a methoxy group, and a formyl group at different positions, making it a member of both anisoles and benzaldehydes. 4-Methoxy-2-(trifluoromethyl)benzaldehyde is known for its diverse reactive properties, which are further enhanced by the stability and unique reactivity imparted by the trifluoromethyl group, establishing it as a valuable synthetic building block.
Uses
Used in Chemical Synthesis:
4-Methoxy-2-(trifluoromethyl)benzaldehyde is used as a synthetic building block for the creation of various complex organic molecules. Its unique reactivity and stability contribute to the development of new compounds with potential applications in various fields.
Used in Biochemical Research:
In biochemical research, 4-Methoxy-2-(trifluoromethyl)benzaldehyde serves as a valuable compound for studying the interactions and reactions of different biomolecules. Its diverse functional groups allow for a wide range of experimental applications, contributing to the advancement of scientific understanding in biochemistry.
Used in Pharmaceutical Applications:
4-Methoxy-2-(trifluoromethyl)benzaldehyde is utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. Its unique properties and reactivity make it suitable for the development of new pharmaceutical compounds with potential therapeutic benefits.
Used in the Chemical Industry:
4-Methoxy-2-(trifluoromethyl)benzaldehyde is employed in the chemical industry for the production of specialty chemicals and materials. Its versatility and reactivity enable the creation of new products with specific properties, catering to the needs of various market segments.
Check Digit Verification of cas no
The CAS Registry Mumber 106312-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106312-36:
(8*1)+(7*0)+(6*6)+(5*3)+(4*1)+(3*2)+(2*3)+(1*6)=81
81 % 10 = 1
So 106312-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O2/c1-14-7-3-2-6(5-13)8(4-7)9(10,11)12/h2-5H,1H3
106312-36-1Relevant articles and documents
Synthesis of novel structurally simplified estrogen analogues with electron-donating groups in ring A
Tietze, Lutz F.,Vock, Carsten A.,Krimmelbein, Ilga K.,Nacke, Linda
experimental part, p. 2040 - 2060 (2009/12/27)
A library of 25 novel estrogen analogues were prepared in five to eight steps from mostly commercially available substituted anisoles via bromination, formylation, Corey-Fuchs reaction, elimination, and Sonogashira reaction. Georg Thieme Verlag Stuttgart.
