106312-36-1 Usage
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.
Ring-Substituted y1,2-Bis(4-hydroxyphenyl)ethylenediamine>dichloroplatinum(II) Complexes: Compounds with a Selective Effect on the Hormone-Dependent Mammary Carcinoma
Karl, Johann,Gust, Ronald,Spruss, Thilo,Schneider, Martin R.,Schoenenberg, Helmut,et al.
, p. 72 - 83 (2007/10/02)
dichloroplatinum(II) complexes with one substituent in the 2-position (CH3, CF3, F, Br, I: meso- and dl-1-PtCl2, meso-(3-5)-PtCl2, meso-(7 and 8)-PtCl2) or two substituents in the 2,6-position (CH3, Cl: meso-2-PtCl2, meso- and dl-6-PtCl2) in both benzene rings were synthesized and tested for estrogenic and toxic activities.Two complexes (meso-6-PtCl2 and meso-7-PtCl2) possess both effects.In comparative tests on estrogen receptor positive and negative mammary tumors in cell culture (MCF 7, ER+ and MDA-MB 231, ER-) and in animals (MXT, ER+ and MXT, ER-, mouse), meso-6-PtCl2 shows a selective effect on the estrogen receptor positive mammary carcinoma.A further increase of efficacy was achieved with the water-soluble (sulfato)platinum(II) derivative (meso-6-PtSO4).On the DMBA-induced hormone dependent mammary carcinoma of the SD rat, meso-6-PtSO4 is significantly more active than its ligand (meso-6) and cisplatin.
