Cas 1338575-67-9,N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide

1338575-67-9

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Basic information

Product Name: N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide
Synonyms: N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide
CAS NO:1338575-67-9
Molecular Formula:
Molecular Weight: 314.319
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: N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide(1338575-67-9)
EPA Substance Registry System: N-((4-methyl-5-oxotetrahydrofuran-2-yl)methyl)-4-nitrobenzenesulfonamide(1338575-67-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1338575-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1338575-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,5,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338575-67:
(9*1)+(8*3)+(7*3)+(6*8)+(5*5)+(4*7)+(3*5)+(2*6)+(1*7)=189
189 % 10 = 9
So 1338575-67-9 is a valid CAS Registry Number.

1338575-67-9Upstream product

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1338575-67-9Relevant academic research and scientific papers

Copper-catalyzed iminoiodane-mediated aminolactonization of Olefins: Application to the synthesis of 5,5-disubstituted butyrolactones

Karila, Delphine,Leman, Loic,Dodd, Robert H.

, p. 5830 - 5833 (2011)

A copper(I)-catalyzed reaction of a variety of 4-aryl-pent-4-enoates with nosyliminoiodane generated in situ provides the corresponding 5-aryl-5-nosylamidomethylbutyrolactones. The reaction presumably proceeds via an aziridine intermediate, which could be

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