500770-83-2 Usage
Uses
Used in Pharmaceutical Research:
BOC-(S)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is used as a key intermediate in the synthesis of various bioactive compounds, contributing to the development of new drugs. Its unique structure allows for the creation of diverse pharmaceutical agents with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, BOC-(S)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID serves as a versatile building block, enabling the construction of complex organic molecules with specific functionalities. Its presence of reactive groups facilitates various chemical reactions, expanding the scope of synthetic chemistry.
Used in Medicinal Chemistry:
BOC-(S)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is employed as a research tool in medicinal chemistry, aiding in the exploration of structure-activity relationships and the optimization of drug candidates. Its unique structural features provide insights into the design and synthesis of novel therapeutic agents.
Used in Agrochemical Development:
BOC-(S)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID also finds application in the development of agrochemicals, where its potential as a building block for bioactive compounds can be harnessed to create new pesticides or herbicides with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 500770-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 500770-83:
(8*5)+(7*0)+(6*0)+(5*7)+(4*7)+(3*0)+(2*8)+(1*3)=122
122 % 10 = 2
So 500770-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(19)15-10(8-12(17)18)9-6-4-5-7-11(9)16(20)21/h4-7,10H,8H2,1-3H3,(H,15,19)(H,17,18)
500770-83-2Relevant academic research and scientific papers
Temporary electrostatic impairment of DNA recognition: Light-driven DNA binding of peptide dimers
Jiménez-Balsa, Adrián,Pazos, Elena,Martínez-Albardonedo, Borja,Mascare?as, José L.,Vázquez, M. Eugenio
supporting information; experimental part, p. 8825 - 8829 (2012/10/08)
Appending negatively charged Glu8 tails to a peptide dimer derived from the GCN4 transcription factor leads to an effective suppression of its DNA binding. The specific DNA recognition can be restored by irradiation with UV light by using a pho
Photolytic control of peptide self-assembly
Bosques, Carlos J.,Imperiali, Barbara
, p. 7530 - 7531 (2007/10/03)
Herein, we present a methodology that allows for the temporal control of fibrillization of amyloidogenic peptides. This general approach implements a photolabile linker that connects the amyloidogenic peptide to a fibril-inhibitory unit, in this case, a p
