112229-51-3 Usage
Uses
Used in Pharmaceutical Development:
Z-D-Orn-OH is utilized as a pharmaceutical precursor for the development of new drugs, particularly those targeting metabolic disorders and protein synthesis pathways. Its unique structure and properties make it a valuable component in the design and synthesis of innovative therapeutic agents.
Used in Research and Development:
In the field of biological research, Z-D-Orn-OH is employed as a research tool to study the structure and function of biological molecules. Its incorporation into peptides and proteins allows scientists to investigate the effects of amino acid modifications on protein folding, stability, and function.
Used in Organic Synthesis:
Z-D-Orn-OH is used as a building block in the synthesis of complex organic compounds, such as pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique side chain configuration and reactivity make it a versatile component in organic synthesis processes.
Used in Metabolic Studies:
In the field of metabolism, Z-D-Orn-OH is used to study the urea cycle and the biosynthesis of proteins. Its role in these processes provides insights into the regulation of nitrogen balance and protein synthesis, which are essential for understanding various metabolic disorders and developing targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 112229-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,2 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112229-51:
(8*1)+(7*1)+(6*2)+(5*2)+(4*2)+(3*9)+(2*5)+(1*1)=83
83 % 10 = 3
So 112229-51-3 is a valid CAS Registry Number.
112229-51-3Relevant academic research and scientific papers
An alternative synthesis of N5-Acetyl-N5-hydroxy-L-ornithine from L-Ornithine
Milewska,Chimiak
, p. 233 - 234 (2007/10/02)
N5-Acetyl-N5-hydroxy-L-ornithine is obtained from L-ornithine in 20% overall yield via oxidation of the ω-amino group in N2-benzyloxycarbonyl-L-ornithine tert-butyl ester with dibenzoyl peroxide and subsequent N5-acetylation.
