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Naphtho[1,8-b,c]thiopyran, also known as benzo[b]thiophene, is a heterocyclic organic compound consisting of a benzene ring fused to a thiophene ring. It has the molecular formula C10H8S and is characterized by the presence of a sulfur atom in the thiophene ring. naphtho<1,8-b,c>thiopyran is an aromatic molecule with a planar structure, and it exhibits various chemical properties due to the presence of both aromatic and heteroatom characteristics. Naphtho[1,8-b,c]thiopyran is an important building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds, as well as a precursor for the production of dyes and pigments. Its unique structure and reactivity make it a valuable compound in the field of organic chemistry and materials science.

203-93-0

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203-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203-93-0 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 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 203-93:
(5*2)+(4*0)+(3*3)+(2*9)+(1*3)=40
40 % 10 = 0
So 203-93-0 is a valid CAS Registry Number.

203-93-0Downstream Products

203-93-0Relevant academic research and scientific papers

HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXXVII. THERMAL REACTIONS OF 1-NAPHTHYLTHIYL RADICALS WITH ACETYLENE

Russavskaya, N. V.,Sukhomazova, E. N.,Korchevin, N. A.,Deryagina, E. N.,Voronkov, M. G.

, p. 1531 - 1534 (2007/10/02)

Naphthylthiyl radicals 1-C10H7S, generated during the thermolysis of 1-C10H7SH, (1-C10H7)2S2, and 1-C10H7SCH2CH=CH2 and also from the 1-C10H7X-H2S system (X = Cl, Br), react with acetylene at 410-700 deg C, forming naphthothiophene and naphthothiopyran.Under certain conditions the yield of each of these difficulty obtainable heterocycles under certain conditions amounts to 47 and 60percent respectively.

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