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β-benzyloxycarbonylaminopivaloyl-β-aminopivaloyl-β-aminopivalic acid ethyl ester is a complex organic compound with the molecular formula C23H36N2O6. It is a derivative of β-aminopivalic acid, featuring a β-benzyloxycarbonyl group and an additional β-aminopivaloyl moiety. β-benzyloxycarbonylaminopivaloyl-β-aminopivaloyl-β-aminopivalic acid ethyl ester is characterized by its ester functional group, which is attached to an ethyl group. It is synthesized for use in peptide synthesis, where it serves as a protected building block. The benzyl group provides a temporary protection for the amino group, which can be removed under specific conditions when the peptide chain is complete. β-benzyloxycarbonylaminopivaloyl-β-aminopivaloyl-β-aminopivalic acid ethyl ester is significant in the field of medicinal chemistry and drug development due to its potential applications in creating novel peptide-based therapeutics.

80253-40-3

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80253-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80253-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80253-40:
(7*8)+(6*0)+(5*2)+(4*5)+(3*3)+(2*4)+(1*0)=103
103 % 10 = 3
So 80253-40-3 is a valid CAS Registry Number.

80253-40-3Relevant academic research and scientific papers

Synthesis of β-Amino-acid Peptides. Part 2. Preparation of Peptides of 2-Amino-2,2-dimethylpropionic Acid by Means of Conventional Coupling Reagents and with Oxazin-6-one Derivatives

Drey, Charies N.C.,Ridge, Richard J.

, p. 2468 - 2471 (2007/10/02)

Side reactions were encountered during the coupling of 3-amino-2,2-dimethylpropionic acid (β-Api) derivatives, some of which could be directly ascribed to steric hindrance at the carboxy-group.Protected and deprotected tri- and hexa-peptides were prepared

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