Cas 1297848-03-3,3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one

1297848-03-3

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Basic information

Product Name: 3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one
Synonyms: 3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one
CAS NO:1297848-03-3
Molecular Formula:
Molecular Weight: 478.432
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: 3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one(1297848-03-3)
EPA Substance Registry System: 3-(bis(4-(dimethylamino)phenyl)methyl)-5-bromo-3-methylindolin-2-one(1297848-03-3)

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: 1297848-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1297848-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,8,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1297848-03:
(9*1)+(8*2)+(7*9)+(6*7)+(5*8)+(4*4)+(3*8)+(2*0)+(1*3)=213
213 % 10 = 3
So 1297848-03-3 is a valid CAS Registry Number.

1297848-03-3Upstream product

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1297848-03-3Relevant academic research and scientific papers

Alkylation of oxazolones and related heterocycles through an SN1 reaction

Alba, Andrea-Nekane R.,Calbet, Teresa,Font-Bardia, Merce,Moyano, Albert,Rios, Ramon

experimental part, p. 2053 - 2056 (2011/05/16)

The alkylation of oxazolones through an SN1 reaction by using stabilized carbocations is reported. The reaction (catalyzed by Bronsted acids, such as TFA or thioureas) affords the final compounds in excellent yields. Reaction with other heteroc

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