75304-18-6 Usage
Uses
Used in Pharmaceutical Research and Development:
Acetamide, N-[(2-aminophenyl)sulfonyl]is used as a building block for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Compound Production:
This chemical compound is utilized as an intermediate in the production of a wide range of organic compounds, playing a crucial role in the synthesis of various chemical products.
Used in Medicinal Chemistry and Drug Discovery:
Acetamide, N-[(2-aminophenyl)sulfonyl]has potential applications in the field of medicinal chemistry and drug discovery, where it can be employed to explore new chemical entities and develop innovative therapeutic approaches.
Used in Chemical Synthesis:
In the chemical synthesis industry, Acetamide, N-[(2-aminophenyl)sulfonyl]is used as a versatile intermediate, enabling the production of a variety of chemical products and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 75304-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75304-18:
(7*7)+(6*5)+(5*3)+(4*0)+(3*4)+(2*1)+(1*8)=116
116 % 10 = 6
So 75304-18-6 is a valid CAS Registry Number.
75304-18-6Relevant academic research and scientific papers
ALLOSTERIC CHROMENONE INHIBITORS OF PHOSPHOINOSITIDE 3-KINASE (PI3K) FOR THE TREATMENT OF DISEASES ASSOCIATED WITH P13K MODULATION
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Paragraph 1255, (2021/10/11)
The disclosure relates to compounds of Formula (I) as allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) useful in the treatment of diseases or disorders associated with PI3K modulation, Formula (I), or a prodrug, solvate, enantiomer, st
Iridium-Catalyzed ortho-C?H Amidation of Benzenesulfonamides with Sulfonyl Azides
Hou, Hongcen,Zhao, Yongli,Sheng, Shouri,Chen, Junmin
, p. 4393 - 4398 (2019/08/28)
We developed herein an iridium-catalyzed direct C?H activation/ C?N bond formation reaction of benzenesulfonamides with sulfonyl azides. The amidation reaction provides a protocol for the synthesis of 2-aminobenzesulfonamides in good to excellent yields. This strategy features a wide substrate scope, tolerates a broad range of functional groups under external oxidant-free conditions and only releases molecular nitrogen as the sole by-product. Moreover, the preliminary mechanism was investigated and the proposed reaction pathway was provided. (Figure presented.).
