Cas 1383926-93-9,(Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide

1383926-93-9

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Basic information

Product Name: (Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide
Synonyms: (Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide
CAS NO:1383926-93-9
Molecular Formula:
Molecular Weight: 728.525
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: (Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide(1383926-93-9)
EPA Substance Registry System: (Z)-N-(4-bromophenyl)-N-((2-(N-(4-bromophenyl)-4-methylphenylsulfonamido)-3-methylenecyclobutylidene)methyl)-4-methylbenzenesulfonamide(1383926-93-9)

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: 1383926-93-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1383926-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,9,2 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1383926-93:
(9*1)+(8*3)+(7*8)+(6*3)+(5*9)+(4*2)+(3*6)+(2*9)+(1*3)=199
199 % 10 = 9
So 1383926-93-9 is a valid CAS Registry Number.

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1383926-93-9Relevant academic research and scientific papers

Phosphite-gold(I)-catalyzed [2+2] intermolecular cycloaddition of enol ethers with N-allenylsulfonamides

Suarez-Pantiga, Samuel,Hernandez-Diaz, Cristina,Piedrafita, Maria,Rubio, Eduardo,Gonzalez, Jose M.

, p. 1651 - 1657 (2012/08/08)

Addition of catalytic amounts of a phosphite-based gold(I) catalyst efficiently triggers the intermolecular [2+2] cycloaddition of allenes and alkenes substituted by electron-donor groups. The reaction is fast and furnishes cyclobutane derivatives in a st

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