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β-benzyloxycarbonylaminopivaloyl-β-aminopivaloyl-β-aminopivalic acid is a complex organic compound with the molecular formula C21H32N2O6. It is a tripeptide derivative, consisting of three amino acids: β-aminopivalic acid, β-aminopivaloyl, and β-benzyloxycarbonylaminopivaloyl. The compound is characterized by the presence of a benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. The structure of β-benzyloxycarbonylaminopivaloyl-β-aminopivaloyl-β-aminopivalic acid features a central β-aminopivalic acid core, with the other two amino acids attached to it through amide bonds. This specific arrangement of amino acids and the presence of the Cbz group make it a unique and valuable compound in the field of peptide chemistry, with potential applications in drug development and chemical research.

80253-41-4

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80253-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80253-41-4 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 80253-41:
(7*8)+(6*0)+(5*2)+(4*5)+(3*3)+(2*4)+(1*1)=104
104 % 10 = 4
So 80253-41-4 is a valid CAS Registry Number.

80253-41-4Relevant 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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