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2,3-Cyclopentenopyridine, 97%|100141|533-37-9

2,3-Cyclopentenopyridine, 97%

Cat. No JKH08296_5_G
J&K Chemical

Product Information

Product Name
2,3-Cyclopentenopyridine, 97%
Brand Name
J&K
Product Number
100141
CAS
533-37-9
Molecular Formula
C8H9N
Molecular Weight
119.17
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
6,7-dihydro-5H-cyclopenta(b)pyridine
PubChem CID
68292
IUPAC Name
6,7-dihydro-5H-cyclopentabpyridine
InChI Key
KRNSYSYRLQDHDK-UHFFFAOYSA-N
SMILES
C1CC2=C(C1)N=CC=C2

Properties

Density
1.018
Boiling Point
87-88
Flash Point
67
n20D
1.5440

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

C-H alkylation of pyridines with olefins catalyzed by imidazolin-2-iminato-ligated rare-earth alkyl complexes
Publication Name: Science China Chemistry
Publication Date: 2023-05-10
DOI: 10.1007/s11426-023-1588-8

Novel multicomponent synthesis of 6,7-dihydro-5H-cyclopenta[b]pyridine derivatives
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2020-12
DOI: 10.1007/s10593-020-02854-7

Gold Vinylidenes as Useful Intermediates in Synthetic Organic Chemistry
Publication Name: Synthesis
Publication Date: 2019-01-10
DOI: 10.1055/s-0037-1611647

Oxidation of Six-Membered Hetarenes To Give N-Oxides
Publication Name: Science of Synthesis
Publication Date: 2017

Oxyfunctionalization of pyridine derivatives using whole cells of Burkholderia sp. MAK1
Publication Name: Scientific Reports
Publication Date: 2016-12-16
DOI: 10.1038/srep39129

2,3-Cyclopentenopyridine, 97%

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