501015-24-3 Usage
Uses
Used in Organic Synthesis:
Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is used as a building block for the synthesis of complex organic molecules. Its unique structure allows for the creation of a variety of chemical entities with potential applications in different industries.
Used in Peptide Chemistry:
In peptide chemistry, Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is employed as a key component in the assembly of peptides and peptide mimetics. The Boc protecting group ensures that the amino group remains unreactive until specifically deprotected, enabling the synthesis of peptides with precise sequences and structures.
Used in Pharmaceutical Research:
Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is utilized in pharmaceutical research as a precursor for the development of new drugs. Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid's unique chemical and potential biological properties make it a valuable tool for the design and synthesis of therapeutic agents.
Used in Chemical Research:
In the realm of chemical research, Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is applied to explore novel chemical reactions and mechanisms. The presence of the nitrophenyl group provides a platform for studying its reactivity and potential applications in various chemical processes.
Used in the Development of Peptide-based Drug Delivery Systems:
Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is used as a component in the design of peptide-based drug delivery systems. Its unique structure allows for the development of systems that can improve the delivery, bioavailability, and therapeutic outcomes of various drugs.
Used in the Synthesis of Bioactive Peptides:
Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid is employed in the synthesis of bioactive peptides, which have potential applications in medicine, agriculture, and other fields. Boc-(R)-3-amino-3-(3-nitro-phenyl)-propanoic acid's unique properties can contribute to the development of peptides with specific biological activities and therapeutic potentials.
Check Digit Verification of cas no
The CAS Registry Mumber 501015-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 501015-24:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*5)+(2*2)+(1*4)=73
73 % 10 = 3
So 501015-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(19)15-11(8-12(17)18)9-5-4-6-10(7-9)16(20)21/h4-7,11H,8H2,1-3H3,(H,15,19)(H,17,18)
501015-24-3Relevant articles and documents
CYTOSTATIC CONJUGATES WITH INTEGRIN LIGANDS
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Page/Page column 8; 19, (2020/06/01)
The present invention relates to novel pharmaceutical compounds comprising of an αvβ3 integrin antagonist, a linking unit comprising of L-Val – L-Pro – L-Asp cleavable by elastase, a polyethyleneglycol (PEG) spacer and a cytotoxic element, to processes for preparation thereof, to the use thereof for treating, preventing or managing diseases and conditions including hyperproliferative disorders such as cancer in humans and other mammals.
