138423-98-0 Usage
Description
N-Acetic acid-indole-3-carboxaldehyde is an organic compound that belongs to the family of indole derivatives. It is a solid substance with a chemical structure that features an indole ring and a carboxylic acid group. N-Acetic acid-indole-3-carboxaldehyde is known for its ability to form a resin through coupling with an amino-resin, which can be utilized for immobilizing amines and their derivatives via reductive amination.
Uses
Used in Chemical Synthesis:
N-Acetic acid-indole-3-carboxaldehyde is used as a key intermediate in the synthesis of various indole-based compounds, which have applications in pharmaceuticals, agrochemicals, and other chemical industries. Its unique chemical structure allows for the formation of a resin, which can be employed in the immobilization of amines and their derivatives through reductive amination.
Used in Analytical Chemistry:
In the field of analytical chemistry, N-Acetic acid-indole-3-carboxaldehyde can be used as a derivatizing agent for the detection and analysis of various compounds, particularly amines. The formation of the indolecarboxaldehyde resin allows for the selective and efficient immobilization of target molecules, enabling their detection and quantification.
Used in Material Science:
N-Acetic acid-indole-3-carboxaldehyde can be utilized in the development of novel materials, such as resins and polymers, due to its ability to form a resin through coupling with an amino-resin. These materials can find applications in various industries, including coatings, adhesives, and composites, where their unique properties can be exploited for specific uses.
Used in Research and Development:
As a versatile organic compound, N-Acetic acid-indole-3-carboxaldehyde can be employed in research and development for the exploration of new chemical reactions, synthesis methods, and potential applications. Its solid-state nature and ability to form a resin make it an attractive candidate for studying various aspects of chemical reactivity and material properties.
Check Digit Verification of cas no
The CAS Registry Mumber 138423-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,2 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138423-98:
(8*1)+(7*3)+(6*8)+(5*4)+(4*2)+(3*3)+(2*9)+(1*8)=140
140 % 10 = 0
So 138423-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c13-7-8-5-12(6-11(14)15)10-4-2-1-3-9(8)10/h1-5,7H,6H2,(H,14,15)
138423-98-0Relevant articles and documents
AMIDES OF ANTHRACYCLINE ANTIBIOTICS AND N-CARBOXYMETHYLASCORBIGEN
Korolev, A. M.,Lazhko, E. I.,Preobrazhenskaya, M. N.,Bal'zarini, Ya.,Klerk, E. De
, p. 805 - 808 (1991)
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New nucleotide-competitive non-nucleoside inhibitors of terminal deoxynucleotidyl transferase: Discovery, characterization, and crystal structure in complex with the target
Costi, Roberta,Cuzzucoli Crucitti, Giuliana,Pescatori, Luca,Messore, Antonella,Scipione, Luigi,Tortorella, Silvano,Amoroso, Alessandra,Crespan, Emmanuele,Campiglia, Pietro,Maresca, Bruno,Porta, Amalia,Granata, Ilaria,Novellino, Ettore,Gouge, Jéro?me,Delarue, Marc,Maga, Giovanni,Di Santo, Roberto
, p. 7431 - 7441 (2013/10/21)
Terminal deoxynucletidyl transferase (TdT) is overexpressed in some cancer types, where it might compete with pol μ during the mutagenic repair of double strand breaks (DSBs) through the nonhomologous end joining (NHEJ) pathway. Here we report the discove
PHAMACEUTICAL PREPARATIONS COMPRISING INSULIN
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Page/Page column 225, (2010/02/15)
Novel preparations comprising ligands for the HisB10 Zn2+ sites of the R-state insulin hexamer wherein the ligand is extended by protamine that are capable of prolonging the ac-tion of insulin preparations.