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5-Benzylsulfanyl-3,4-dihydro-2H-pyrrole is a chemical compound with the molecular formula C11H13NS. It is a heterocyclic compound, specifically a pyrrole derivative, which features a benzylsulfanyl group attached to the 5-position of the pyrrole ring. 5-benzylsulfanyl-3,4-dihydro-2H-pyrrole is characterized by its aromatic nature and the presence of a sulfur atom in the molecule, which can contribute to unique chemical reactivity and properties. It is often used in organic synthesis and as a building block for more complex molecules, particularly in the pharmaceutical and chemical industries. The compound's structure and properties make it a valuable intermediate in the synthesis of various biologically active compounds and materials with potential applications in drug development and other areas of chemistry.

4226-77-1

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4226-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4226-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4226-77:
(6*4)+(5*2)+(4*2)+(3*6)+(2*7)+(1*7)=81
81 % 10 = 1
So 4226-77-1 is a valid CAS Registry Number.

4226-77-1Downstream Products

4226-77-1Relevant academic research and scientific papers

SYNTHESIS, STRUCTURE, AND CHEMICAL PROPERTIES OF TRIMETHYLSILYL DERIVATIVES OF THIOLACTAMS

Sergeev, V. N.,Artamkin, S. A.,Pestunovich, S. V.,Albanov, A. I.,Voronkov, M. G.,Baukov, Yu. I.

, p. 1490 - 1497 (2007/10/02)

Trimethylsilyl derivatives of five-, six-, and seven-membered thiolactams with an N-silyl structure were synthesized for the first time.Their alkylation with primary alkyl halides under comparatively mild conditions occurs at the sulfur atom; the reaction with secondary alkyl halides is accompanied by hydrogen halide elimination, and this becomes the only reaction pathway with tertiary halides.The preparative acylation of N-trimethylsilylthiolactams yields N-acyl derivatives; the intermediate formation of S-acylation products was established by means of low-temperature NMR monitoring.

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