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Benzenemethanesulfonamide, N-butyl-, also known as N-butylbenzenesulfonamide or N-Butylbenzenesulfonamide, is an organic compound with the chemical formula C11H15NO2S. It is a derivative of benzenesulfonamide, where a butyl group (C4H9) is attached to the nitrogen atom. Benzenemethanesulfonamide, N-butyl- is a white crystalline solid and is soluble in organic solvents such as ethanol and acetone. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its versatile chemical structure, it can be further modified to create a range of different compounds with various applications in the chemical industry.

69688-96-6

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69688-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69688-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,8 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69688-96:
(7*6)+(6*9)+(5*6)+(4*8)+(3*8)+(2*9)+(1*6)=206
206 % 10 = 6
So 69688-96-6 is a valid CAS Registry Number.

69688-96-6Downstream Products

69688-96-6Relevant academic research and scientific papers

Benzothiazole Sulfinate: A Sulfinic Acid Transfer Reagent under Oxidation-Free Conditions

Day, Jacob J.,Neill, Deshka L.,Xu, Shi,Xian, Ming

supporting information, p. 3819 - 3822 (2017/07/26)

Sulfinic acids are commonly encountered intermediates found in natural product synthesis and medicinal chemistry. However, because of high reactivity, instability, and harsh reaction conditions, they are difficult to synthesize. Herein we have developed an oxidation-free method to produce sulfinic acids and sulfinate salts using 2-sulfinyl benzothiazole (BTS). We have also demonstrated the synthetic usefulness by developing one-pot syntheses of sulfones and sulfonamides.

A Convenient Synthesis of 5-Substituted Tetrahydro-1,4,3-oxathiazine 4,4-Dioxides

Grunder-Klotz, Evelyne,Humbert, Paul,Ehrhardt, Jean-Daniel

, p. 733 - 742 (2007/10/02)

An adventageous one pot procedure for the synthesis of tetrahydro-1,4,3-oxathiazine 4,4-dioxides by dialkylation of readily available α,N-alkyl or arylsulfonamide dianions with gaseous formaldehyde is reported.Stability and some reactions of these heterocycles are also described.

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