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(2S)-6-benzyloxy-2-tert-butyloxycarbonylaminohexanoic acid is an amino acid derivative with a molecular formula C20H29NO5. It features a chiral center at the 2-position, classifying it as an L-amino acid derivative. (2S)-6-benzyloxy-2-tert-butyloxycarbonylaminohexanoic acid is characterized by the presence of a benzyloxy group and a tert-butyloxycarbonyl (Boc) protecting group, which are significant for its applications in organic synthesis and medicinal chemistry.

200405-50-1

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200405-50-1 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-6-benzyloxy-2-tert-butyloxycarbonylaminohexanoic acid is utilized as a building block for protein synthesis, playing a crucial role in the development of peptides and complex organic molecules. Its unique structure and functional groups make it a valuable component in the synthesis of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2S)-6-benzyloxy-2-tert-butyloxycarbonylaminohexanoic acid is employed as a key intermediate for designing and creating innovative pharmaceuticals. Its Boc protecting group is particularly useful in peptide synthesis, allowing for the stepwise construction of peptide chains with controlled selectivity and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 200405-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,4,0 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 200405-50:
(8*2)+(7*0)+(6*0)+(5*4)+(4*0)+(3*5)+(2*5)+(1*0)=61
61 % 10 = 1
So 200405-50-1 is a valid CAS Registry Number.

200405-50-1Relevant academic research and scientific papers

First total synthesis of the bone resorption markers deoxypyridinoline and hydroxypyridinoline

Waelchli, Rudolf,Beerli,Meigel,Revesz

, p. 2831 - 2836 (2007/10/03)

The first total synthesis of the collagen crosslinks deoxypyridinoline 1 and hydroxypyridinoline 2 was achieved. The key intermediate, pyridine 3 served as starting material for the preparation of compounds 1 and 2 and derivatives of 1. These compounds create optimal tools to establish a diagnostic kit for bone resorption.

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