Cas 1403828-85-2,N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide

1403828-85-2

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Basic information

Product Name: N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide
Synonyms: N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide
CAS NO:1403828-85-2
Molecular Formula:
Molecular Weight: 464.323
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: N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide(1403828-85-2)
EPA Substance Registry System: N-(2-bromocyclohex-2-enyl)-2,2,2-trifluoro-N-[2-(4-methoxybenzyloxy)-1,1-dimethylethyl]acetamide(1403828-85-2)

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: 1403828-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403828-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,8,2 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1403828-85:
(9*1)+(8*4)+(7*0)+(6*3)+(5*8)+(4*2)+(3*8)+(2*8)+(1*5)=152
152 % 10 = 2
So 1403828-85-2 is a valid CAS Registry Number.

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1403828-85-2Relevant academic research and scientific papers

Synthesis of hexahydroindoles by intramolecular C sp 3-H alkenylation: Application to the synthesis of the core of aeruginosins

Sofack-Kreutzer, Julien,Martin, Nicolas,Renaudat, Alice,Jazzar, Rodolphe,Baudoin, Olivier

, p. 10399 - 10402 (2012/11/07)

Give me five: Pd-catalyzed intramolecular C sp 3-H arylations have been successfully extended to alkenylations. This method shows remarkable selectivity and gives synthetically useful hexahydroindoles, as illustrated with the synthesis of the octahydroind

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