Cas 1007893-45-9,1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole

1007893-45-9

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Basic information

Product Name: 1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole
Synonyms: 1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole
CAS NO:1007893-45-9
Molecular Formula:
Molecular Weight: 513.795
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: 1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole(1007893-45-9)
EPA Substance Registry System: 1-benzyl-3-(tert-butyldimethylsiloxy)-5-(2-tert-butyl-4-methylphenoxy)-2-methyl-1H-indole(1007893-45-9)

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: 1007893-45-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007893-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,8,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1007893-45:
(9*1)+(8*0)+(7*0)+(6*7)+(5*8)+(4*9)+(3*3)+(2*4)+(1*5)=149
149 % 10 = 9
So 1007893-45-9 is a valid CAS Registry Number.

1007893-45-9Upstream product

1007893-45-9Downstream Products

1007893-45-9Relevant academic research and scientific papers

Palladium-catalyzed C-O and C-C coupling reactions of electron-rich indoles

Schwarz, Nicolle,Pews-Davtyan, Anahit,Alex, Karolin,Tillack, Annegret,Beller, Matthias

, p. 3722 - 3730 (2008/09/19)

A novel palladium-catalyzed formation of indole aryl ethers is described. In general, the corresponding indole ethers are obtained in the presence of Pd(OAc)2 combined with N-phenyl-2-(di-1-adamantylphosphino)pyrrole in high yields. Georg Thiem

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