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Hexylsulfanyl-diphenyl-acetic acid is a complex organic compound with the chemical formula C18H22O2S. It is characterized by a hexylsulfanyl (hexylthio) group attached to a diphenyl-acetic acid moiety. The hexylsulfanyl group consists of a six-carbon alkyl chain with a sulfur atom at one end, forming a thiol group. The diphenyl-acetic acid part of the molecule features two phenyl rings attached to an acetic acid group. Hexylsulfanyl-diphenyl-acetic acid is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and intermediates. Its unique structure allows for a range of chemical reactions and interactions, making it a valuable component in the development of new compounds with specific therapeutic or industrial properties.

2668-32-8

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2668-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2668-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2668-32:
(6*2)+(5*6)+(4*6)+(3*8)+(2*3)+(1*2)=98
98 % 10 = 8
So 2668-32-8 is a valid CAS Registry Number.

2668-32-8Relevant academic research and scientific papers

SAR studies on the potent and selective muscarinic antagonist 2- ethylthio-2,2-diphenylacetic acid N,N-diethylaminoethyl ester

Scapecchi, Serena,Angeli, Piero,Dei, Silvia,Ghelardini, Carla,Gualtieri, Fulvio,Marucci, Gabriella,Paparelli, Fiorella,Romanelli, M. Novella,Teodori, Elisabetta

, p. 122 - 128 (1997)

Molecular modification of the potent and selective muscarinic antagonist 2-ethylthio-2,2-diphenylacetic acid N,N-diethylaminoethyl ester was performed in order to identify M2 selective antagonists able to cross the blood brain barrier and potentially useful in the treatment of Alzheimer's disease. Modifications included substitution or hydrogenation of one of the phenyl rings as well as their incorporation in a tricyclic system. In general the changes introduced were detrimental for both affinity and selectivity. Only a modest M2 selectivity is present in some compounds that, on the other hand, carry a quaternary ammonium group which precludes their penetration into the brain.

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