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β-Benzyloxycarbonylaminopivaloyl-β-aminopivalic acid is a complex organic compound with the chemical formula C18H26N2O5. It is a derivative of β-aminopivalic acid, featuring a benzyloxycarbonyl (Cbz) protecting group attached to the amino group. β-benzyloxycarbonylaminopivaloyl-β-aminopivalic acid is primarily used in peptide synthesis as a protected amino acid, where the Cbz group serves to prevent unwanted side reactions during the coupling process. The pivaloyl group (Piv) is another protecting group present in this molecule, which can be used to stabilize the peptide backbone. The compound plays a crucial role in the synthesis of various peptides and proteins, particularly in the field of pharmaceuticals and biochemistry, by ensuring the correct sequence and structure of the final product.

80253-39-0

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80253-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80253-39-0 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, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80253-39:
(7*8)+(6*0)+(5*2)+(4*5)+(3*3)+(2*3)+(1*9)=110
110 % 10 = 0
So 80253-39-0 is a valid CAS Registry Number.

80253-39-0Relevant 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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