203915-48-4 Usage
Uses
Used in Pharmaceutical Industry:
3,4'-Bis(trifluoromethyl)benzhydrol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with enhanced properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL serves as a crucial component in the creation of agrochemicals, potentially improving the effectiveness of pesticides and other agricultural chemicals.
Used in Plastics Production:
3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL is utilized as a building block in the production of plastics, where its properties can influence the final plastic's characteristics, such as durability and resistance to environmental factors.
Used in Dyes Industry:
3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL is used as a precursor in the manufacture of dyes, contributing to the colorfastness and vibrancy of the final product.
Used in Perfumery:
3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL is employed in the perfume industry to create unique scents, leveraging its ability to form complex aromatic structures.
Used in Organic Electronics:
Due to its electronic properties, 3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL has potential applications in the field of organic electronics, where it could be used in the development of organic light-emitting diodes (OLEDs) or organic solar cells.
Used in Material Science:
In material science, 3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL is explored for its potential to enhance or create new materials with specific optical, electronic, or structural properties.
It is important to handle 3,4'-BIS(TRIFLUOROMETHYL)BENZHYDROL with care due to its potential toxic or harmful effects if not used properly, emphasizing the need for safety measures in its application across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 203915-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,9,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203915-48:
(8*2)+(7*0)+(6*3)+(5*9)+(4*1)+(3*5)+(2*4)+(1*8)=114
114 % 10 = 4
So 203915-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H10F6O/c16-14(17,18)11-6-4-9(5-7-11)13(22)10-2-1-3-12(8-10)15(19,20)21/h1-8,13,22H
203915-48-4Relevant articles and documents
Traceless directing group for stereospecific nickel-catalyzed alkyl-alkyl cross-coupling reactions
Greene, Margaret A.,Yonova, Ivelina M.,Williams, Florence J.,Jarvo, Elizabeth R.
supporting information; experimental part, p. 4293 - 4296 (2012/09/22)
Stereospecific nickel-catalyzed cross-coupling reactions of benzylic 2-methoxyethyl ethers are reported for the preparation of enantioenriched 1,1-diarylethanes. The 2-methoxyethyl ether serves as a traceless directing group that accelerates cross-coupling. Chelation of magnesium ions is proposed to activate the benzylic C-O bond for oxidative addition.
An electrochemical coupling of organic halide with aldehydes, catalytic in chromium and nickel salts. the Nozaki-Hiyama-Kishi reaction.
Durandetti,Nedelec,Perichon
, p. 2073 - 2076 (2007/10/03)
[reaction: see text] Electrochemical arylation of arenecarboxaldehydes using an iron sacrificial anode in the presence of chromium and nickel catalysts afforded the corresponding arylated secondary alcohols in moderate to good yields. The chromium and nickel salts as catalysts are obtained by oxidation of a stainless steel rod during a preelectrolysis in 7% and 3%, respectively. The process was also applied to the addition of vinyl halide, allyl acetate, or alpha-chloroester to aromatic aldehydes.
Nickel- and chromium-catalysed electrochemical coupling of aryl halides with arenecarboxaldehydes
Durandetti, Muriel,Perichon, Jacques,Nedelec, Jean-Yves
, p. 9009 - 9013 (2007/10/03)
Electrochemical arylation of arenecarboxaldehydes using a stainless steel sacrificial anode in the presence of Ni catalysts afforded the corresponding arylated secondary alcohols in good yields.
