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Z-Arg-OMe, also known as Z-Arginine Methyl Ester, is a synthetic chemical compound derived from the naturally occurring amino acid, L-arginine. The compound is characterized by the presence of a benzyloxycarbonyl (Z) protecting group and a methyl ester (OMe) at the carboxylic acid end. Z-Arg-OMe is widely used in peptide synthesis as a building block, where the Z group serves to protect the amino group from unwanted side reactions, and the OMe group facilitates the coupling process. It plays a crucial role in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs and therapeutics.

6072-05-5

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6072-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6072-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6072-05:
(6*6)+(5*0)+(4*7)+(3*2)+(2*0)+(1*5)=75
75 % 10 = 5
So 6072-05-5 is a valid CAS Registry Number.

6072-05-5Relevant academic research and scientific papers

The Total Synthesis of the Bioactive Natural Product Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B

Fenner, Sabine,Wilson, Zoe E.,Ley, Steven V.

supporting information, p. 15902 - 15912 (2016/10/24)

Herein, we describe our full investigations into the synthesis of the peptide-derived natural product plantazolicin A, a compound that demonstrates promising selective activity against the causative agent of anthrax toxicity, and its biosynthetic precurso

Direct N-glycan profiling in the presence of tryptic peptides on MALDI-TOF by controlled ion enhancement and suppression upon glycan-selective derivatization

Shinohara, Yasuro,Furukawa, Jun-Ichi,Niikura, Kenichi,Miura, Nobuaki,Nishimura, Shin-Ichiro

, p. 6989 - 6997 (2007/10/03)

Even though the formidably laborious and time-consuming nature of oligosaccharide analysis limits certain attempts to analyze the glycosylation profile, the significant elucidation of carbohydrate modifications is largely dependent on it. Aiming to substa

A Mild and Efficient Method for the Preparation of Guanidines

Poss, Michael A.,Iwanowicz, Edwin,Reid, Joyce A.,Lin, James,Gu, Zhengxiang

, p. 5933 - 5936 (2007/10/02)

A mild and efficient method for the preparation of guanidines by reaction of an acylated thiourea with an amine followed by removal of the acyl groups(s) from the intermediate acylguanidine is reported.Key Words: acylguanidine, acylthiourea, guanidine, water soluble carbodiimide

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