Cas 880153-90-2,Carbamic acid, [(1S)-2-[[2-(2,2-dibromoethenyl)-3-methylphenyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester

880153-90-2

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Basic information

Product Name: Carbamic acid, [(1S)-2-[[2-(2,2-dibromoethenyl)-3-methylphenyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester
Synonyms:
CAS NO:880153-90-2
Molecular Formula: C20H20Br2N2O3
Molecular Weight: 496.198
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: Carbamic acid, [(1S)-2-[[2-(2,2-dibromoethenyl)-3-methylphenyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S)-2-[[2-(2,2-dibromoethenyl)-3-methylphenyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester(880153-90-2)
EPA Substance Registry System: Carbamic acid, [(1S)-2-[[2-(2,2-dibromoethenyl)-3-methylphenyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester(880153-90-2)

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: 880153-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 880153-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,0,1,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 880153-90:
(8*8)+(7*8)+(6*0)+(5*1)+(4*5)+(3*3)+(2*9)+(1*0)=172
172 % 10 = 2
So 880153-90-2 is a valid CAS Registry Number.

880153-90-2Upstream product

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880153-90-2Relevant academic research and scientific papers

Cul-catalyzed tandem intramolecular amidation using gem-dibromovinyl systems

Yuen, Josephine,Fang, Yuan-Qing,Lautens, Mark

, p. 653 - 656 (2007/10/03)

Imidazoindolones are present as the key structural motif in the family of antifungals, fumiquinazolines, and the antagonist asperlicin. The first example of a Cul-catalyzed tandem intramolecular amidation forming substituted imidazoindolones from readily

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