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2-phenylpyrrolo[2,1-b][1,3]benzothiazole is a complex organic compound with the molecular formula C18H11NS. It is a heterocyclic molecule that features a pyrrolo[2,1-b][1,3]benzothiazole core, which is a fused ring system consisting of a pyrrole and a benzothiazole. The "2-phenyl" part of the name indicates that a phenyl group (a benzene ring with a hydrogen atom replaced by a methyl group) is attached to the second carbon of the pyrrole ring. 2-phenylpyrrolo[2,1-b][1,3]benzothiazole is known for its potential applications in the field of materials science, particularly as a building block for the synthesis of advanced materials with unique electronic and optical properties. It is also of interest in medicinal chemistry due to its potential as a scaffold for the development of new drugs. The compound's structure endows it with specific chemical and physical properties, making it a subject of study in organic synthesis and chemical research.

1147-93-9

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1147-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1147-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1147-93:
(6*1)+(5*1)+(4*4)+(3*7)+(2*9)+(1*3)=69
69 % 10 = 9
So 1147-93-9 is a valid CAS Registry Number.

1147-93-9Relevant academic research and scientific papers

2-Methylthiazolium Salts as 1,4-Dinucleophiles. Thiazolopyridinium Salts from Westphal Condensation

Galera, C.,Vaquero, J. J.,Navio, Garcia J. L.,Alvarez-Builla, J.

, p. 1889 - 1892 (2007/10/02)

Condensation of 2-methylthiazolium salts with 1,2-dicarbonyls in the presence of base, yielded thiazolopyridinium derivatives.Results with different substrates are discussed.

2-METHYLENE-3-PHENACYLBENZOTHIAZOLINE: DIMERIZATION AND REACTIONS WITH ELECTRON-DEFICIENT ACETYLENES AND OLEFINS

Tsuge, Otohiko,Tanaka, Minoru,Shimoharada, Hiroshi,Noguchi, Michihiko

, p. 1705 - 1712 (2007/10/02)

On treatment with triethylamine in acetonitrile at 0 deg C, 2-methyl-3-phenacylbenzothiazolium bromide gave a dimer of 2-methylene-3-phenacylbenzothiazoline in a quantitative yield.The methylene base, generated in situ, reacted with electron-deficient ace

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