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α-Ethyl ω-benzyl DL-α-aminosuberate hydrochloride is a complex organic compound with the chemical formula C16H26ClNO4. It is a derivative of α-aminosuberate, which is an amino acid analog. α-Ethyl ω-benzyl DL-α-aminosuberate hydrochloride features an ethyl group at the α-position and a benzyl group at the ω-position, with a hydrochloride salt form. It is synthesized for various applications in the pharmaceutical and chemical industries, such as a research tool in studying enzyme interactions and as a potential therapeutic agent. The hydrochloride salt form enhances its solubility and stability, making it suitable for certain biological assays and medicinal applications.

84175-17-7

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84175-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84175-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,7 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84175-17:
(7*8)+(6*4)+(5*1)+(4*7)+(3*5)+(2*1)+(1*7)=137
137 % 10 = 7
So 84175-17-7 is a valid CAS Registry Number.

84175-17-7Relevant academic research and scientific papers

Synthesis of Protected 2-Amino-8-oxo-9,10-epoxydecanoic Acid from 2-Aminosuberic Acid Derivatives

Rich, Daniel H.,Singh, Jasbir,Gardner, Joseph H.

, p. 432 - 434 (2007/10/02)

A method is reported for synthesizing derivatives of 2-amino-8-oxo-9,10-epoxydecanoic acid (Aoe) from 2-aminosuberic acid (Asu) derivatives under conditions that do not disrupt peptide bonds.The epoxy ketone amino acid Aoe is found in three biologically active cyclic peptides.Ethyl 2-(acetylamino)suberate was converted to ethyl 2-DL-(acetylamino)-8-oxo-(RS)-9,10-epoxydecanoate in 45-50 percent yield by sequential reactions with phosphorus pentachloride followed by reaction with tetravinyltin and benzylchlorobis(triphenylphosphine)palladium(II) to give the vinyl ketone in 70 percent yield.Epoxidation of enone with tert-butyl hydroperoxide using triton B as catalyst gave the N-acetyl ethyl ester of Aoe in 70 percent yield.Methods for preparing protected 2-aminosuberic acid derivatives from glycine ester benzal imine are also described.

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