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Z-L-Leu-L-Lys(Boc)-OH*dicyclohexylamine is a complex chemical compound that consists of a peptide sequence with two amino acids, L-Leucine (L-Leu) and L-Lysine (L-Lys), connected by a peptide bond. The L-Lysine residue is protected with a tert-butyloxycarbonyl (Boc) group, which is a common strategy in peptide synthesis to prevent unwanted side reactions. The compound is further associated with dicyclohexylamine, which acts as a base to facilitate the deprotection of the Boc group under certain conditions. Z-L-Leu-L-Lys(Boc)-OH*dicyclohexylamine is typically used in the synthesis of larger peptides or proteins, where the Boc group is used to protect the amino group of lysine during the assembly process, and dicyclohexylamine is used to remove this protecting group at a later stage. The "Z" in the name refers to the benzyloxycarbonyl group, which is another protecting group for the N-terminal amino group of the peptide, ensuring that the peptide chain grows in a controlled manner.

95049-85-7

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95049-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95049-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,4 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95049-85:
(7*9)+(6*5)+(5*0)+(4*4)+(3*9)+(2*8)+(1*5)=157
157 % 10 = 7
So 95049-85-7 is a valid CAS Registry Number.

95049-85-7Downstream Products

95049-85-7Relevant academic research and scientific papers

Total Synthesis of Thymosin β4, 1. - Conventional Synthesis of the Fragment of Thymosin β4

Kapurniotu, Afroditi,Voelter, Wolfgang

, p. 1251 - 1258 (2007/10/02)

As part of the total synthesis of thymosin β4 two synthetic pathways for the synthesis of the thymosin β4 fragment are described.The side-chain functions are protected by tert-butyl and the α-amino residues by Z groups.As tem

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