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Benzenepropanethioic acid, α-[(triphenylmethyl)amino]-, S-2-pyridinyl ester, (S)- is a complex organic compound with the chemical formula C31H28N2O2S. It is a chiral molecule, with the (S)-configuration indicating the presence of a stereocenter. Benzenepropanethioic acid, a-[(triphenylmethyl)amino]-, S-2-pyridinyl ester, (S)- is characterized by a benzenepropanethioic acid backbone, which is modified with an α-[(triphenylmethyl)amino] group and an S-2-pyridinyl ester moiety. The triphenylmethyl group provides a bulky, electron-donating substituent, while the 2-pyridinyl ester group introduces a heteroaromatic ring and a potential site for nucleophilic attack. Benzenepropanethioic acid, a-[(triphenylmethyl)amino]-, S-2-pyridinyl ester, (S)- may be of interest in the fields of organic synthesis, medicinal chemistry, and materials science due to its unique structural features and potential applications in the development of pharmaceuticals or other specialty chemicals.

112839-75-5

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112839-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112839-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112839-75:
(8*1)+(7*1)+(6*2)+(5*8)+(4*3)+(3*9)+(2*7)+(1*5)=125
125 % 10 = 5
So 112839-75-5 is a valid CAS Registry Number.

112839-75-5Relevant academic research and scientific papers

Synthesis and biological activity of ketomethylene-containing nonapeptide analogues of snake venom angiotensin converting enzyme inhibitors

Almquist,Chao,Judd,Mitoma,Rossi,Panasevich,Matthews

, p. 561 - 567 (1988)

Two ketomethylene-containing nonapeptide analogues were synthesized to determine if ketomethylene analogues of the nonapeptide venom inhibitors of angiotensin converting enzyme (ACE) would have oral ACE inhibition activity. Both ketomethylene-containing n

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