Cas 389635-01-2,9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1<sup>3,7</sup>]heneicosa-3,5,7<sup>(21)</sup>,16,18,19-hexaene

389635-01-2

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Product Name: 9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1^3,7]heneicosa-3,5,7⁽²¹⁾,16,18,19-hexaene
Synonyms: 9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1^3,7]heneicosa-3,5,7⁽²¹⁾,16,18,19-hexaene
CAS NO:389635-01-2
Molecular Formula:
Molecular Weight: 537.7
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: 9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1^3,7]heneicosa-3,5,7⁽²¹⁾,16,18,19-hexaene(CAS DataBase Reference)
NIST Chemistry Reference: 9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1^3,7]heneicosa-3,5,7⁽²¹⁾,16,18,19-hexaene(389635-01-2)
EPA Substance Registry System: 9,12-dioxo-2-oxa-10-butyl-11-hexyl-14-ethoxycarbonyl-18-amino-10,13-diazatricyclo[14.2.2.1^3,7]heneicosa-3,5,7⁽²¹⁾,16,18,19-hexaene(389635-01-2)

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Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 389635-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 389635-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 389635-01:
(8*3)+(7*8)+(6*9)+(5*6)+(4*3)+(3*5)+(2*0)+(1*1)=192
192 % 10 = 2
So 389635-01-2 is a valid CAS Registry Number.

389635-01-2Upstream product

42564-51-2 4-fluoro-3-nitrobenzaldehyde

389635-01-2Downstream Products

389635-01-2Relevant academic research and scientific papers

A rapid access to biaryl ether containing macrocycles by pairwise use of Ugi 4CR and intramolecular S(N)Ar-based cycloetherification.

Cristau,Vors,Zhu

, p. 4079 - 4082 (2007/10/03)

[reaction: see text] From readily accessible starting materials, macrocycles with an endo aryl-aryl ether bond are synthesized in only two operations by combination of the Ugi four-component reaction and an intramolecular S(N)Ar reaction. The nitro group serves as an activator for the macrocyclization and provides a handle for the introduction of functional group diversity. A Ugi reaction promoted by ammonium chloride in aprotic solvent is documented for the first time.

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