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N′-(4-methoxyphenylsulfonyl)-N,N-dimethylformimidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1344029-97-5

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1344029-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1344029-97-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,0,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1344029-97:
(9*1)+(8*3)+(7*4)+(6*4)+(5*0)+(4*2)+(3*9)+(2*9)+(1*7)=145
145 % 10 = 5
So 1344029-97-5 is a valid CAS Registry Number.

1344029-97-5Downstream Products

1344029-97-5Relevant academic research and scientific papers

A Novel Synthesis of N -Sulfonylformamidines from N Sulfonyl sulfonamides

Jeong, Yuri,Ban, Jaeyoung,Lim, Minkyung,Rhee, Hakjune

, p. 1867 - 1874 (2018)

N -Sulfonylformamidines were synthesized from N -sulfonylsulfonamides by reacting with p -toluenesulfonyl chloride (TsCl) and N, N - disubstituted formamides. In this reaction, it was expected that mixing TsCl with the N, N -disubstituted formamide would generate an iminium salt (Vilsmeier reagent). The reaction avoids the use of metal catalysts and hazardous reagents, and the desired N -sulfonylformamidines were obtained in 60% to quantitative yields.

Preparation method of sulfonyl amidine with 2-Picolylamine and DMF-DMA as amine sources

-

Paragraph 0074; 0076, (2020/09/09)

The invention discloses a preparation method of sulfonyl amidine with 2-Picolylamine and DMF-DMA as amine sources. The method comprises the following steps: reacting sulfonyl chloride with 2-Picolylamine to obtain an intermediate product; and then reacting the intermediate product with DMF-DMA in the presence of a catalyst at a temperature of 60-100 DEG C, then performing cooling to room temperature, extracting the reaction solution with ethyl acetate, performing layering, drying and then concentrating to obtain a target product sulfonyl amidine. According to the method disclosed by the invention, the reaction of secondary sulfonamide and DMF-DMA is realized, and the synthesis path of sulfonyl amidine is expanded. The synthetic reaction is simple in operation, mild in condition and convenient in post-treatment, and the obtained intermediate product and the product are high in purity and yield.

Otherwise inert reaction of sulfonamides/carboxamides with formamides via proton transfer-enhanced reactivity

Niu, Zaihai,Lin, Shaoxia,Dong, Zhiyong,Sun, Hao,Liang, Fushun,Zhang, Jingping

, p. 2460 - 2465 (2013/06/04)

NBS-mediated addition-elimination reaction of sulfonamides/carboxamides and formamides afforded N-sulfonylamidines and N-formylarylamides, respectively, depending on the different mechanism of elimination. Hydrogen bond-induced proton transfer leads to en

Direct condensation of sulfonamide and formamide: NaI-catalyzed synthesis of N-sulfonyl formamidine using TBHP as oxidant

Chen, Shulin,Xu, Yuan,Wan, Xiaobing

supporting information; experimental part, p. 6152 - 6155 (2012/01/03)

A new N-sulfonyl formamidine synthesis was developed via NaI-catalyzed direct condensation of sulfonamide and formamide. The green methodology is featured by high atom economy, easily available starting materials, the lack of need for a transition-metal c

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