948995-62-8 Usage
Description
Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is a bifunctional linker reagent used in bioconjugation and protein labeling applications. It is a chemical compound that can react with primary amines to form stable amide bonds. The succinimidyl group allows the reagent to couple with proteins, peptides, and other molecules, while the nitrobenzyloxy group can be used for cleavage and release of the labeled target. Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is often utilized in research and diagnostics to create stable and efficient protein conjugates for various biological and medical purposes.
Uses
Used in Bioconjugation Applications:
Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is used as a bifunctional linker reagent for bioconjugation, enabling the coupling of proteins, peptides, and other molecules with primary amines to form stable amide bonds.
Used in Protein Labeling Applications:
In protein labeling, Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is used as a reagent to label proteins and peptides, allowing for the creation of stable and efficient protein conjugates for various biological and medical purposes.
Used in Research and Diagnostics:
Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is used in research and diagnostics as a tool to create stable protein conjugates, which can be utilized for various biological and medical applications, including the development of diagnostic assays and therapeutic agents.
Used in Cleavage and Release of Labeled Targets:
The nitrobenzyloxy group in Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate can be used for the cleavage and release of the labeled target, making it a useful reagent in applications where controlled release of the labeled molecule is required.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is used as a reagent for the development of drug conjugates, which can improve the targeting and delivery of therapeutic agents to specific cells or tissues.
Used in Biotechnology Industry:
In the biotechnology industry, Succinimidyl 4-[3,5-Dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyrate is used as a tool for the creation of protein conjugates, which can be employed in various applications such as the development of biosensors, diagnostic assays, and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 948995-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,9,9 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 948995-62:
(8*9)+(7*4)+(6*8)+(5*9)+(4*9)+(3*5)+(2*6)+(1*2)=258
258 % 10 = 8
So 948995-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H22N2O8/c1-14-11-17(19(26)7-10-22(29)33-24-20(27)8-9-21(24)28)12-15(2)23(14)32-13-16-3-5-18(6-4-16)25(30)31/h3-6,11-12H,7-10,13H2,1-2H3
948995-62-8Relevant articles and documents
Concise synthesis of photocleavable molecular tag for laser desorption ionization mass spectrometry via fries reaction
Gathirwa, Jeremiah W.,Maki, Toshihide
, p. 1016 - 1022 (2013/02/25)
A new synthetic route for the photocleavable molecular tag for laser desorption ionization mass spectrometry (LDI-MS) was achieved using the Fries reaction of 2,6-dimethylphenyl ester as its key reaction. Zirconium chloride was used as uniquely efficient
