Cas 666819-45-0,5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one

666819-45-0

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Basic information

Product Name: 5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one
Synonyms: 5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one
CAS NO:666819-45-0
Molecular Formula: C27H22BrN3O
Molecular Weight: 484.38708
EINECS: N/A
Product Categories: N/A
Mol File: 666819-45-0.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one(666819-45-0)
EPA Substance Registry System: 5-bromo-3,3-bis(1-methyl-1H-indol-3-yl)-1-methyl-1,3-dihydro-2H-indol-2-one(666819-45-0)

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: 666819-45-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 666819-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,8,1 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 666819-45:
(8*6)+(7*6)+(6*6)+(5*8)+(4*1)+(3*9)+(2*4)+(1*5)=210
210 % 10 = 0
So 666819-45-0 is a valid CAS Registry Number.

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666819-45-0Relevant articles and documents

Catalytic asymmetric synthesis of substituted 3-hydroxy-2oxindoles

Hanhan, Nadine V.,Sahin, Aziza H.,Chang, Toby W.,Fettinger, James C.,Franz, Annaliese K.

scheme or table, p. 744 - 747 (2010/04/06)

Chemical equation presented Chemical equation presented No more double trouble: The competing double-addition pathway was suppressed when chiral scandium(III) and indium (III) complexes were used to catalyze the addition of indoles and other π nucleophile

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