Cas 1454880-49-9,N-[4-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide

1454880-49-9

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Basic information

Product Name: N-[4-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide
Synonyms: N-[4-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide
CAS NO:1454880-49-9
Molecular Formula:
Molecular Weight: 446.408
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-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide(1454880-49-9)
EPA Substance Registry System: N-[4-bromo-2-{5-(tert-butyl)-2-methylphenyl}naphthalen-1-yl]methanesulfonamide(1454880-49-9)

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: 1454880-49-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454880-49-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,8,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1454880-49:
(9*1)+(8*4)+(7*5)+(6*4)+(5*8)+(4*8)+(3*0)+(2*4)+(1*9)=189
189 % 10 = 9
So 1454880-49-9 is a valid CAS Registry Number.

1454880-49-9Upstream product

1454880-49-9Downstream Products

1454880-49-9Relevant academic research and scientific papers

Organocatalytic C-H/C-H' cross-biaryl coupling: C-selective arylation of sulfonanilides with aromatic hydrocarbons

Ito, Motoki,Kubo, Hiroko,Itani, Itsuki,Morimoto, Koji,Dohi, Toshifumi,Kita, Yasuyuki

supporting information, p. 14078 - 14081 (2013/10/21)

The hypervalent iodine-mediated C-C selective coupling of N-methanesulfonyl anilides with aromatic hydrocarbons has been developed. The first organocatalytic oxidative cross-biaryl-coupling was achieved by the catalyst control in defining specific 2,2′-diiodobiphenyls for the direct C-C bond formations.

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