64724-23-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Amino-5-chloro-3-iodobenzoic acid is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique combination of functional groups allows for the development of new drugs with potential therapeutic benefits. The presence of the amino group, chlorine, and iodine atoms provides opportunities for further chemical modifications, enhancing the compound's pharmacological properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Amino-5-chloro-3-iodobenzoic acid serves as a versatile building block. Its reactivity and structural features enable the formation of a wide array of organic compounds, which can be applied in various chemical processes and industries. 2-AMINO-5-CHLORO-3-IODOBENZOIC ACID's ability to participate in a range of chemical reactions, such as substitution, addition, and condensation, makes it a valuable asset in the synthesis of complex organic molecules.
Used in Chemical Industry:
2-Amino-5-chloro-3-iodobenzoic acid finds applications in the chemical industry, where it can be employed as a precursor for the production of various specialty chemicals. Its unique structure and reactivity contribute to the development of new materials with specific properties, such as dyes, pigments, and other functional compounds. 2-AMINO-5-CHLORO-3-IODOBENZOIC ACID's potential in the chemical industry is further expanded by its ability to be modified and incorporated into larger molecular structures, offering a broad range of applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 64724-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64724-23:
(7*6)+(6*4)+(5*7)+(4*2)+(3*4)+(2*2)+(1*3)=128
128 % 10 = 8
So 64724-23-8 is a valid CAS Registry Number.
64724-23-8Relevant academic research and scientific papers
Screening for covalent inhibitors using DNA-display of small molecule libraries functionalized with cysteine reactive moieties
Zambaldo,Daguer,Saarbach,Barluenga,Winssinger
supporting information, p. 1340 - 1351 (2016/07/21)
DNA-encoded chemical libraries are increasingly used to identify leads for drug discovery or chemical biology. Despite the resurging interest in covalent inhibitors, libraries are typically designed with synthon filtered out for reactive functionalities that can engage a target through covalent interactions. Herein, we report the synthesis of two libraries containing Michael acceptors to identify cysteine reactive ligands. We developed a simple procedure to discriminate between covalent and high affinity non-covalent inhibitors using DNA display of the library in a microarray format. The methodology was validated with known covalent and high affinity non-covalent kinase inhibitors. Screening of the library revealed novel covalent inhibitors for MEK2 and ERBB2.
HYDRAZIDE COMPOUND AND PESTICIDAL USE OF THE SAME
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Page/Page column 538-539, (2008/06/13)
A hydrazide compound represented by the formula (1): has excellent pesticidal activity.
