Cas 106544-19-8,2-(1-cyano-2-phenylcyclopropyl)-5-(ethoxycarbonyl)-4,5,6,11b-tetrahydro-Δ<sup>4</sup>-1,2,4-oxadiazolino<3,2-a>-β-carboline

106544-19-8

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Basic information

Product Name: 2-(1-cyano-2-phenylcyclopropyl)-5-(ethoxycarbonyl)-4,5,6,11b-tetrahydro-Δ⁴-1,2,4-oxadiazolino<3,2-a>-β-carboline
Synonyms:
CAS NO:106544-19-8
Molecular Formula:
Molecular Weight: 426.475
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: 2-(1-cyano-2-phenylcyclopropyl)-5-(ethoxycarbonyl)-4,5,6,11b-tetrahydro-Δ⁴-1,2,4-oxadiazolino<3,2-a>-β-carboline(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1-cyano-2-phenylcyclopropyl)-5-(ethoxycarbonyl)-4,5,6,11b-tetrahydro-Δ⁴-1,2,4-oxadiazolino<3,2-a>-β-carboline(106544-19-8)
EPA Substance Registry System: 2-(1-cyano-2-phenylcyclopropyl)-5-(ethoxycarbonyl)-4,5,6,11b-tetrahydro-Δ⁴-1,2,4-oxadiazolino<3,2-a>-β-carboline(106544-19-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 106544-19-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106544-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,4 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106544-19:
(8*1)+(7*0)+(6*6)+(5*5)+(4*4)+(3*4)+(2*1)+(1*9)=108
108 % 10 = 8
So 106544-19-8 is a valid CAS Registry Number.

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106544-19-8Relevant academic research and scientific papers

Employment of Nitriles in the Stereoselective Cycloaddition to Nitrones

Plate, Ralf,Hermkens, Pedro H. H.,Smits, Jan M. M.,Nivard, Rutger J. F.,Ottenheijm, Haary C. J.

, p. 1047 - 1051 (2007/10/02)

The cycloaddition of the nitrones 8-11 to the geminal dinitriles 12a-d has been evaluated.Under thermal as well high-pressure reaction conditions 1,3 dipolar cycloadditions proceed with complete regioselectivity to give the Δ4-1,2,4-oxadiazolin

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