Cas 1421692-67-2,2-(1-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate

1421692-67-2

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Basic information

Product Name: 2-(1-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate
Synonyms: 2-(1-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate
CAS NO:1421692-67-2
Molecular Formula:
Molecular Weight: 491.587
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-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate(1421692-67-2)
EPA Substance Registry System: 2-(1-(phenoxycarbonyl)-1,2,5,6-tetrahydropyridin-2-yl)-1,3-phenylene dibenzoate(1421692-67-2)

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: 1421692-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1421692-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,6,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1421692-67:
(9*1)+(8*4)+(7*2)+(6*1)+(5*6)+(4*9)+(3*2)+(2*6)+(1*7)=152
152 % 10 = 2
So 1421692-67-2 is a valid CAS Registry Number.

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1421692-67-2Relevant academic research and scientific papers

Direct site-selective arylation of enamides via a decarboxylative cross-coupling reaction

Gigant, Nicolas,Chausset-Boissarie, La?titia,Gillaizeau, Isabelle

supporting information, p. 816 - 819 (2013/03/28)

An efficient Pd-catalyzed decarboxylative cross-coupling reaction of simple enamides was achieved. Depending on the choice of the nitrogen-protecting group, a site-selective synthesis of mono- or diarylated framework(s) was performed under mild conditions

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