Cas 1343480-27-2,N-[4-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide

1343480-27-2

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Basic information

Product Name: N-[4-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide
Synonyms: N-[4-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide
CAS NO:1343480-27-2
Molecular Formula:
Molecular Weight: 493.58
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-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide(1343480-27-2)
EPA Substance Registry System: N-[4-(1,4-dimethoxy-2-naphthalenyl)-3,5-dimethoxyphenyl]-4-methylbenzenesulfonamide(1343480-27-2)

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: 1343480-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1343480-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,3,4,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1343480-27:
(9*1)+(8*3)+(7*4)+(6*3)+(5*4)+(4*8)+(3*0)+(2*2)+(1*7)=142
142 % 10 = 2
So 1343480-27-2 is a valid CAS Registry Number.

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1343480-27-2Relevant academic research and scientific papers

Metal-free C-H cross-coupling toward oxygenated naphthalene-benzene linked biaryls

Dohi, Toshifumi,Ito, Motoki,Itani, Itsuki,Yamaoka, Nobutaka,Morimoto, Koji,Fujioka, Hiromichi,Kita, Yasuyuki

supporting information; experimental part, p. 6208 - 6211 (2012/01/06)

The intermolecular C-H cross-coupling between aromatic ethers has been achieved for the first time using perfluorinated hypervalent iodine(III) compounds as extreme single-electron-transfer (SET) oxidants. The demonstrations of this specific coupling coul

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