Cas 1360557-01-2,dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate

1360557-01-2

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Basic information

Product Name: dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate
Synonyms: dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate
CAS NO:1360557-01-2
Molecular Formula:
Molecular Weight: 375.372
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: dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(1360557-01-2)
EPA Substance Registry System: dimethyl 3-(3,5-difluorophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate(1360557-01-2)

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: 1360557-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360557-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,5,5 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1360557-01:
(9*1)+(8*3)+(7*6)+(6*0)+(5*5)+(4*5)+(3*7)+(2*0)+(1*1)=142
142 % 10 = 2
So 1360557-01-2 is a valid CAS Registry Number.

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1360557-01-2Relevant academic research and scientific papers

A serendipitous discovery: Nickel catalyst for the cycloaddition of diynes with unactivated nitriles

Kumar, Puneet,Prescher, Simon,Louie, Janis

, p. 10694 - 10698 (2011)

In the nick of time! The catalytic combination of [Ni(cod)2] (cod=1,5-cyclooctadiene) and the ligand 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene (Xantphos) was used to access pyridines (see scheme). The reaction proceeds under ambient cond

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