61714-76-9 Usage
Uses
Used in Pharmaceutical Industry:
3-methyl-2-thiophenesulfonyl chloride is used as a synthetic reagent for the production of various pharmaceuticals. Its application is primarily due to its ability to introduce the thiophene sulfonyl chloride group into organic molecules, which is crucial for the synthesis of certain drug compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 3-methyl-2-thiophenesulfonyl chloride is utilized as a key intermediate in the synthesis of sulfonylurea herbicides. Its role is vital for the creation of these herbicidal compounds, which are widely used in agriculture for effective weed control.
Used in Organic Synthesis:
3-methyl-2-thiophenesulfonyl chloride is employed as a reagent in organic synthesis for the introduction of the thiophene sulfonyl chloride group into a variety of organic molecules. This modification can enhance the properties of these molecules, making them suitable for various applications in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 61714-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61714-76:
(7*6)+(6*1)+(5*7)+(4*1)+(3*4)+(2*7)+(1*6)=119
119 % 10 = 9
So 61714-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClO2S2/c1-4-2-3-9-5(4)10(6,7)8/h2-3H,1H3
61714-76-9Relevant academic research and scientific papers
Quinazolinone Compound and Application Thereof
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Paragraph 0285-0287, (2020/11/27)
The present invention relates to a series of quinazolinone compounds and applications thereof as PI3Kα inhibitors. In particular, the present invention relates to a compound shown in formula (I) and a tautomer or pharmaceutically acceptable salt thereof.
Sulfonylureas: A new class of cancer chemotherapeutic agents
Mohamadi,Spees,Grindey
, p. 3012 - 3016 (2007/10/02)
This study summarizes the antitumor properties of a number of sulofenur thiophene analogs against subcutaneously implanted 6C3HED lymphosarcoma with structural modification of the aryl moiety of the sulfonamide portion of the diarylsulfonylureas. The spectrum of activity of N-(p-chlorophenyl)-N'-[(5- methoxy-2-thienyl)sulfonyl]urea in the HXGC3, VRC5, CX-1, and LX-1 cell lines is also presented.
