1007893-41-5 Usage
Structure
1H-Indole-1-carboxylic acid, 5-(2-methylphenoxy)-, 1,1-dimethylethyl ester
Synonyms
tert-butyl 5-(o-tolyl)indole-1-carboxylate
Physical state
Pale yellow solid
Molecular weight
349.43 g/mol
Usage
Building block in the synthesis of pharmaceuticals and agrochemicals, primarily used in medicinal chemistry research and has potential applications in the development of new drugs for various therapeutic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 1007893-41-5 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 1007893-41:
(9*1)+(8*0)+(7*0)+(6*7)+(5*8)+(4*9)+(3*3)+(2*4)+(1*1)=145
145 % 10 = 5
So 1007893-41-5 is a valid CAS Registry Number.
1007893-41-5Relevant articles and documents
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
