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Acenaphtho[1,2-c]thiophene is a heterocyclic aromatic compound with the chemical formula C12H8S. It is a derivative of acenaphthylene, where one of the carbon atoms is replaced by a sulfur atom, forming a thiophene ring. acenaphtho[1,2-c]thiophene is characterized by its unique electronic properties and is of interest in the field of organic chemistry and materials science. Acenaphtho[1,2-c]thiophene is known for its potential applications in the development of organic semiconductors, such as in the creation of thin-film transistors and organic light-emitting diodes (OLEDs), due to its ability to form stable π-conjugated systems. The compound's structure and properties make it a promising candidate for further research and development in the area of advanced materials.

206-20-2

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206-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206-20-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 206-20:
(5*2)+(4*0)+(3*6)+(2*2)+(1*0)=32
32 % 10 = 2
So 206-20-2 is a valid CAS Registry Number.

206-20-2Downstream Products

206-20-2Relevant academic research and scientific papers

Functionalization of conductive poly(thiophenes) and poly(pyrroles)

Ono, Noboru,Tsukamura, Chikanori,Nomura, Youta,Hotta, Syunsuke,Murashima, Takashi,Ogawa, Takuji

, p. 419 - 420 (2007/10/03)

New methods for functionalization of conductive poly(thiophenes) and poly(pyrroles) using fused aromatics or crown ethers are discussed.

Synthesis of Acenaphthoheterocycles and Spiro

Lefkaditis, D. A.,Nicolaides, D. N.,Papageorgiou, G. K.,Stephanidou-Stephanatou, J.

, p. 227 - 230 (2007/10/02)

Methyl (Z)-(1,2-dihydro-2-oxo-1-acenaphthylenylidene)acetate 1 gives with hydroxylamine the oximes 2 and the pyrrole derivative 4, whereas with hydrazines affords the pyridazinones 5 and 6.A pyridazine derivative 8 is also isolated from the reaction of (1,2-dihydro-2-oxo-1-acenaphthylenylidene)acetone 7 with hydrazine hydrate.Reaction between the spiro-derivative 9 and hydroxylamine hydrochloride gives oxime 10, whereas Wittig olefination of 9 with ylide 11 yields compound 12 which by reaction with 2,4,6-trimethylbenzonitrile oxide (13) affords the dispiro-derivatives 14.Finally from the reaction of acenaphthylene-1,2-quinone (17) with the bisylide 16 the acenaphthothiophene (18) is formed.

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