Cas 595577-65-4,Benzenesulfonamide, N-[1-(2-furanyl)-2-methylpropyl]-4-methyl-

595577-65-4

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Product Name: Benzenesulfonamide, N-[1-(2-furanyl)-2-methylpropyl]-4-methyl-
Synonyms:
CAS NO:595577-65-4
Molecular Formula: C15H19NO3S
Molecular Weight: 293.387
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzenesulfonamide, N-[1-(2-furanyl)-2-methylpropyl]-4-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-[1-(2-furanyl)-2-methylpropyl]-4-methyl-(595577-65-4)
EPA Substance Registry System: Benzenesulfonamide, N-[1-(2-furanyl)-2-methylpropyl]-4-methyl-(595577-65-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 595577-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 595577-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,5,5,7 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 595577-65:
(8*5)+(7*9)+(6*5)+(5*5)+(4*7)+(3*7)+(2*6)+(1*5)=224
224 % 10 = 4
So 595577-65-4 is a valid CAS Registry Number.

595577-65-4Upstream product

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595577-65-4Relevant academic research and scientific papers

Manganese=Catalyzed Achmatowicz Rearrangement Using Green Oxidant H2O2

Xing, Qingzhao,Hao, Zhe,Hou, Jing,Li, Gaoqiang,Gao, Ziwei,Gou, Jing,Li, Chaoqun,Yu, Binxun

, p. 9563 - 9586 (2021/07/20)

Oxidation reactions have been extensively studied in the context of the transformations of biomass=derived furans. However, in contrast to the vast literature on utilizing the stoichiometric oxidants, such as m=CPBA and NBS, catalytic methods for the oxidative furan=recyclizations remain scarcely investigated. Given this, we report a means of manganese=catalyzed oxidations of furan with low loading, achieving the Achmatowicz rearrangement in the presence of hydrogen peroxide as an environmentally benign oxidant under mild conditions with wide functional group compatibility.

Synthesis of 3-sulfonyloxypyridines: Oxidative ring expansion of α-furyl-sulfonamides and N→O sulfonyl transfer

Hodgson, Robert,Kennedy, Andrew,Nelson, Adam,Perry, Alexis

, p. 1043 - 1046 (2008/02/13)

N-Sulfonyl pyridinones derived from α-furylsulfonamides may be aromatised with concomitant N→O sulfonyl transfer to produce 3-sulfonyloxypyridines. Georg Thieme Verlag Stuttgart.

Synthesis of 2-aza-1-cyano-4-hydroxyanthraquinones

Claessens, Sven,Jacobs, Jan,De Kimpe, Norbert

, p. 741 - 744 (2008/01/06)

Phthalide annulation of 2-alkylpyridin-3-ones results in the formation of the unexpected 2-aza-1-cyano-4-hydroxy-anthraquinones, the cyano moiety originating from the 3-cyanophthalide. These compounds hold great potential against Epstein-Barr Virus Early

An efficient synthesis of furyl sulfonamides from the reaction of furan with in situ generated N-tosyl imines

Padwa, Albert,Zanka, Atsuhiku,Cassidy, Michael P.,Harris, Joel M.

, p. 4939 - 4944 (2007/10/03)

Treatment of an aldehyde and furan with N-sulfinyl-p-toluenesulfonamide/zinc chloride leads to the formation of furyl sulfonamides via an in situ generated N-tosyl imine intermediate. In one case, a novel 4-tosylamino-5,6-dihydro-4H-3-oxa-benz[e]azulene w

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