Cas 1423075-93-7,(Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate

1423075-93-7

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Basic information

Product Name: (Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate
Synonyms: (Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate
CAS NO:1423075-93-7
Molecular Formula:
Molecular Weight: 420.465
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: (Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate(1423075-93-7)
EPA Substance Registry System: (Z)-3-(1H-indol-3-yl)-1-(2-oxooxazolidin-3-yl)but-1-en-1-yl 2-(4-methoxyphenyl)acetate(1423075-93-7)

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: 1423075-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1423075-93-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,0,7 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1423075-93:
(9*1)+(8*4)+(7*2)+(6*3)+(5*0)+(4*7)+(3*5)+(2*9)+(1*3)=137
137 % 10 = 7
So 1423075-93-7 is a valid CAS Registry Number.

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1423075-93-7Relevant academic research and scientific papers

Gold-catalysed cascade rearrangements of ynamide propargyl esters

Heffernan, Stephen J.,Beddoes, James M.,Mahon, Mary F.,Hennessy, Alan J.,Carbery, David R.

, p. 2314 - 2316 (2013)

The Au(i)-catalysed rearrangement of propargylic esters formed from an ynamide has been studied. The reaction is facile, and when conducted in the presence of a reactive indole nucleophile, leads to a cascade process whereby γ-indolyl α-acyloxyenamides are formed in good yield and excellent E-stereoselectivity. The Royal Society of Chemistry.

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