Cas 1401322-82-4,dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate

1401322-82-4

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Basic information

Product Name: dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate
Synonyms: dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate
CAS NO:1401322-82-4
Molecular Formula:
Molecular Weight: 470.352
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: dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(1401322-82-4)
EPA Substance Registry System: dibenzyl 3-(dichloromethyl)-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(1401322-82-4)

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: 1401322-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401322-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,3,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1401322-82:
(9*1)+(8*4)+(7*0)+(6*1)+(5*3)+(4*2)+(3*2)+(2*8)+(1*2)=94
94 % 10 = 4
So 1401322-82-4 is a valid CAS Registry Number.

1401322-82-4Upstream product

3018-12-0 dichloroacetonitrile

1401322-82-4Downstream Products

1401322-82-4Relevant academic research and scientific papers

Efficient generation of pyridines by ruthenium carbene mediated [2 + 2 + 2] cyclotrimerization

Medina, Sandra,Dominguez, Gema,Perez-Castells, Javier

, p. 4982 - 4985,4 (2012)

Hoveyda-Grubbs' catalyst is able to catalyze crossed [2 + 2 + 2] cyclotrimerizations of diynes with nitriles. Pyridines are obtained with excellent yields when using activated nitriles and low to moderate yields with nonactivated nitriles which are unreac

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