501015-23-2 Usage
Uses
Used in Pharmaceutical Industry:
BOC-(R)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of molecules with specific therapeutic properties, addressing various medical conditions.
Used in Chemical Synthesis:
In the chemical synthesis industry, BOC-(R)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is utilized as a versatile building block for the preparation of a wide array of chemical compounds. Its reactivity and structural features make it suitable for creating complex molecules with diverse applications.
Used in Medicinal Chemistry Research:
BOC-(R)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is employed as a research tool in medicinal chemistry. It aids scientists in understanding the structure-activity relationships of potential drug candidates and contributes to the advancement of drug discovery processes.
Used in Drug Discovery:
BOC-(R)-3-AMINO-3-(2-NITRO-PHENYL)-PROPIONIC ACID is used in drug discovery as a precursor to potential therapeutic agents. Its incorporation into drug molecules can lead to the development of novel treatments for various diseases and disorders, highlighting its importance in the pharmaceutical sector.
Check Digit Verification of cas no
The CAS Registry Mumber 501015-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 501015-23:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*5)+(2*2)+(1*3)=72
72 % 10 = 2
So 501015-23-2 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)
501015-23-2Relevant articles and documents
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
