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93198-68-6

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93198-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93198-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93198-68:
(7*9)+(6*3)+(5*1)+(4*9)+(3*8)+(2*6)+(1*8)=166
166 % 10 = 6
So 93198-68-6 is a valid CAS Registry Number.

93198-68-6Relevant articles and documents

Cerium(IV) ammonium nitrate mediated nitration of coumarins

Ganguly,Sukai,De

, p. 301 - 309 (2001)

A new convenient method of nitration of coumarins using cerium(IV) ammonium nitrate (CAN) has been developed. Higher regioselectivity is observed with CAN and hydrogen peroxide in aqueous medium in comparison with CAN in acetic acid for nitration of 7-hydroxycoumarin, 7-hydroxy-4-methylcoumarin and their derivatives.

Synthesis of 7-Azido-3-Formylcoumarin – A Key Precursor in Bioorthogonally Applicable Fluorogenic Dye Synthesis

Pünk?sti, Zoltán,Kele, Péter,Herner, András

supporting information, p. 1183 - 1188 (2018/03/21)

Coumarins represent an important group of natural products and a common part of various drugs and fluorescent dyestuffs. Herein, we present the synthesis of a coumarin that can serve as a key starting material in the design and synthesis of bioorthogonally applicable fluorogenic dyes. The synthesis of 7-azido-3-formylcoumarin started from 7-diallylaminocoumarin. This allyl protected aminocoumarin is otherwise hard to obtain by conventional methods but was conveniently accessed in good yields by a sequential, Wittig-reaction–UV isomerization process. This sequential approach was studied in more details and applied for the synthesis of a series of substituted coumarins even in one-pot.

3-Trifluoromethylated Coumarins and Carbostyrils by Radical Trifluoromethylation of ortho-Functionalized Cinnamic Esters

Chaabouni, Slim,Simonet, Florent,Fran?ois, Alison,Abid, Souhir,Galaup, Chantal,Chassaing, Stefan

supporting information, p. 271 - 277 (2017/01/24)

A method for the trifluoromethylation of ortho-hydroxycinnamic esters was developed to achieve the regioselective synthesis of 3-trifluoromethylated coumarins. The reaction was performed by using the Togni reagent as the CF3source under mild conditions and showed good functional- group tolerance. The scope of this copper-mediated method was further expanded to the synthesis of 3-trifluoromethylated carbostyrils starting from ortho-aminocinnamic derivatives. Interestingly, a sequential one-pot synthesis of 3-trifluoromethylated coumarins starting from salicylaldehydes was further developed. The mechanism of this cascade reaction was explored, and a radical pathway was found to be consistent with the obtained results.

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