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4-Brom-N-methoxy-benzolsulfonamid, also known as 4-bromo-N-methoxybenzenesulfonamide, is a chemical compound with the molecular formula C7H8BrNO3S. It is a derivative of benzenesulfonamide, featuring a bromine atom at the 4-position, a methoxy group (-OCH3) attached to the nitrogen atom, and a sulfonamide functional group. 4-Brom-N-methoxy-benzolsulfonamid is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through the reaction of 4-bromobenzenesulfonyl chloride with methanol in the presence of a base. The compound is a white crystalline solid and is sensitive to moisture, requiring storage under dry conditions.

3665-10-9

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3665-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3665-10-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3665-10:
(6*3)+(5*6)+(4*6)+(3*5)+(2*1)+(1*0)=89
89 % 10 = 9
So 3665-10-9 is a valid CAS Registry Number.

3665-10-9Downstream Products

3665-10-9Relevant academic research and scientific papers

Palladium-Catalyzed ortho-Benzoylation of Sulfonamides through C?H Activation: Expedient Synthesis of Cyclic N-Sulfonyl Ketimines

Ojha, Subhadra,Panda, Niranjan

, p. 561 - 571 (2019/12/24)

The ortho-carbonylation of sulfonylarenes by non-hazardous aryl aldehydes as a carbonyl precursor was reported. In this method, the sulfonamide group serves as a directing group for C?H activation in the presence of a Pd catalyst under ligand-free conditions. The scope of this strategy has been extended to the one-pot two-step synthesis of cyclic N-sulfonyl ketimines under mild reaction conditions. Our approach could be considered as an alternative by circumventing the use of highly reactive organolithium or Grignard reagents to access a wide range of biologically potent cyclic N-sulfonyl ketimines. (Figure presented.).

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