2304-98-5 Usage
Description
Z-ARG(NO2)-OH, also known as N-(Cbenzyloxycarbonyl)-L-arginine 4-nitrophenylester, is a synthetic compound utilized as a building block in peptide chemistry. It is characterized by its white powder form and possesses unique chemical properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
Z-ARG(NO2)-OH is used as a building block for the synthesis of various peptides and peptide-based drugs. Its application in this industry is due to its ability to facilitate the creation of complex peptide structures that can be used for therapeutic purposes.
Used in Research and Development:
In the field of research and development, Z-ARG(NO2)-OH is used as a key component in the design and synthesis of novel peptides with potential applications in medicine, biotechnology, and other related fields. Its role in this industry is to enable the exploration of new peptide sequences and their potential functions.
Used in Chemical Synthesis:
Z-ARG(NO2)-OH is also used as a reagent in chemical synthesis processes, particularly in the production of various organic compounds and materials. Its application in this industry is attributed to its unique chemical properties that allow for specific reactions and transformations.
Used in Analytical Chemistry:
In analytical chemistry, Z-ARG(NO2)-OH is employed as a reference compound or standard for the development and validation of analytical methods and techniques. Its use in this industry is due to its well-defined chemical structure and properties, which make it an ideal candidate for comparison and calibration purposes.
Overall, Z-ARG(NO2)-OH is a versatile compound with a wide range of applications across various industries, primarily due to its unique chemical properties and its role as a building block in peptide chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2304-98-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2304-98:
(6*2)+(5*3)+(4*0)+(3*4)+(2*9)+(1*8)=65
65 % 10 = 5
So 2304-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H19N5O6/c15-13(18-19(23)24)16-8-4-7-11(12(20)21)17-14(22)25-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9H2,(H,17,22)(H,20,21)(H3,15,16,18)
2304-98-5Relevant articles and documents
Improved selective protections of L-arginine
Moynihan, Humphrey A.,Yu, Weiping
, p. 17 - 23 (2007/10/03)
Reliable procedures for the selective introduction of carbobenzyloxy and phthalimido groups onto the α-amino position, and of carboethoxy groups onto the δ- and ω-guanidino positions of L-arginine are described.
Isolation and characterization of Nα-Benzyloxycarbonyl amino Acid Urethane Hydrolase II from Lactobacillus fermenti 36 ATCC 9338
Matsamura, Eiko,Yamamoto, Eiko,Kawano, Tatsu,Shin, Takashi,Murao, Sawao
, p. 1563 - 1572 (2007/10/02)
A novel enzyme, which was named Nα-benzloxycarbonyl amino acid urethane hydrolase II, was purified from a cell-free extract of Lactobacillus fermenti 36ATCC 9338.The enzyme catalyzed the stoichiometric hydrplysis of N-α-benzyloxycarbonyl arginine to form benzyl alcohol and arginine.The enzyme was purified 106-fold with an activity yield of 3percent.The purified enzyme was homogeneous by disc gel electrophoresis.The molecular weight of native enzyme is about 200,000 by gel filtration, and a molecular weight of 27,000 was found for the reduced and denaturated enzyme was 5.0, it was inhibited by disodium ethylenediamine tetraacetate and p-chloromercuribenzoate, and the presence of a divalent cation, i.e.Co2+, is essential for its activity.
