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4-((2-aminophenyl)thio)-3-fluorobenzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

214483-59-7

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214483-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214483-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,4,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214483-59:
(8*2)+(7*1)+(6*4)+(5*4)+(4*8)+(3*3)+(2*5)+(1*9)=127
127 % 10 = 7
So 214483-59-7 is a valid CAS Registry Number.

214483-59-7Relevant academic research and scientific papers

A Facile Synthesis of Cyanophenothiazines

Marivingt-Mounir, Cecile,Mettey, Yvette,Vierfond, Jean-Michel

, p. 843 - 845 (1998)

A one-pot synthesis of 1, 3 and 4-cyanophenothiazines and a two-step approach to 2-cyanoisomer have been developed. The condensation of 2-aminobenzenethiol and 2,3 or 3,4-dihalogenobenzonitriles followed by Smiles rearrangement or by intramolecular aromatic substitution gave the desired ring systmes.

Efficient and regioselective synthesis of phenothiazine via ferric citrate catalyzed C-S/C-N cross-coupling

Das, Tonmoy Chitta,Quadri, Syed Aziz Imam,Farooqui, Mazahar

supporting information, p. 16 - 24 (2019/05/04)

Efficient C-S and C-N cross-coupling reactions have been developed for regioselective, scalable and environmentally benign synthesis of substituted phenothiazine derivatives. Cross-coupling reactions were demonstrated on various challenging substrates using non-toxic, highly economical, readily available ferric citrate as a catalyst to get desired product with high regioselectivity. Atom economy is the added advantage of this protocol since additional N-protection step before coupling and eventual deprotection of the same to obtain the desired product arenot required. To the best of our knowledge, this is the first report on the use of inexpensive ferric citrate as a catalyst without involving any ligand for the synthesis of regioselectively substituted phenothiazine.

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