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1528-30-9

1528-30-9 | METHYLENECYCLOPENTANE

CAS No: 1528-30-9 Catalog No: AG003S3X MDL No:MFCD00001421

Product Description

Catalog Number:
AG003S3X
Chemical Name:
METHYLENECYCLOPENTANE
CAS Number:
1528-30-9
Molecular Formula:
C6H10
Molecular Weight:
82.1436
MDL Number:
MFCD00001421
IUPAC Name:
methylidenecyclopentane
InChI:
InChI=1S/C6H10/c1-6-4-2-3-5-6/h1-5H2
InChI Key:
NFJPEKRRHIYYES-UHFFFAOYSA-N
SMILES:
C=C1CCCC1
EC Number:
216-203-4

Properties

Complexity:
54.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
82.078g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
82.146g/mol
Monoisotopic Mass:
82.078g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  

Literature

Title Journal
A synthesis of echinopine B. Angewandte Chemie (International ed. in English) 20120723
Brønsted base/Lewis acid cooperative catalysis in the enantioselective Conia-ene reaction. Journal of the American Chemical Society 20090708
Palladium-catalyzed asymmetric [3 + 2] trimethylenemethane cycloaddition reactions. Journal of the American Chemical Society 20061018
Mechanism of the diphenyldisulfone-catalyzed isomerization of alkenes. Origin of the chemoselectivity: experimental and quantum chemistry studies. Journal of the American Chemical Society 20060621
Thermal chemistry of 1-methyl-1-cyclopentene and methylene cyclopentane on Pt(111) surfaces: evidence for double-bond isomerization. The journal of physical chemistry. B 20060518
Coordination copolymerization of severely encumbered isoalkenes with ethylene: enhanced enchainment mediated by binuclear catalysts and cocatalysts. Journal of the American Chemical Society 20051026
Mechanistic investigations of the ethylene tetramerisation reaction. Journal of the American Chemical Society 20050803
A study of vinyl radical cyclization using N-alkenyl-7-bromo-substituted hexahydroindolinones. The Journal of organic chemistry 20050121
Polysulfones: solid organic catalysts for the chemoselective cleavage of methyl-substituted allyl ethers under neutral conditions. Chemical communications (Cambridge, England) 20041107
Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones. Organic letters 20040318
Palladium(II) acetate mediated oxidative cyclization of omega-unsaturated alpha-cyano ketones. A facile methylenecyclopentane annulation process. Chemical communications (Cambridge, England) 20031007
Ultrafast dynamics of cyclohexene and cyclohexene-d10 excited at 200 nm. Journal of the American Chemical Society 20010725
Ruthenium(II)-catalyzed isomer-selective cyclization of 1,6-dienes leading to exo-methylenecyclopentanes: unprecedented cycloisomerization mechanism involving ruthenacyclopentane(hydrido) intermediate. Journal of the American Chemical Society 20010704

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