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Pyridine, 2,3,4,5-tetrahydro-6-[(phenylmethyl)thio]-, also known as 6-benzylthio-2,3,4,5-tetrahydro-1H-pyridine, is an organic compound with the molecular formula C13H17NS. It is a derivative of pyridine, a heterocyclic aromatic compound containing a nitrogen atom in a six-membered ring. This specific compound features a tetrahydro (four hydrogen atoms) pyridine ring with a benzylthio (phenylmethyl sulfanyl) group attached at the 6th position. The presence of the benzylthio group imparts unique chemical and physical properties to the molecule, making it useful in various applications, such as pharmaceuticals and chemical research.

4226-78-2

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4226-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4226-78-2 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 4226-78:
(6*4)+(5*2)+(4*2)+(3*6)+(2*7)+(1*8)=82
82 % 10 = 2
So 4226-78-2 is a valid CAS Registry Number.

4226-78-2Downstream Products

4226-78-2Relevant articles and documents

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.

Treatment of ulcers and hypertension

-

, (2008/06/13)

The invention concerns the treatment of ulcers and hypersecretion in a mammal using compounds of the formula I where Ar is phenyl, which may be substituted or cycloalkyl of 5 to 7 carbon atoms, A is saturated or unsaturated lower alkylene which may be

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