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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Spiro[4.5]decan-6-one

O=C1CCCCC21CCCC2 Request for Quotation
Chemical Name: Spiro[4.5]decan-6-one
CAS Number: 13388-94-8
Product Number: AG00717A(AGN-PC-0JPBJA)
Synonyms:
MDL No:
Molecular Formula: C10H16O
Molecular Weight: 152.2334

Identification/Properties

Computed Properties
Molecular Weight:
152.237g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
152.12g/mol
Monoisotopic Mass:
152.12g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Spiro[4.5]decan-6-one is a versatile compound widely used in chemical synthesis for its unique structural properties and reactivity. This bicyclic ketone serves as a valuable building block in organic chemistry, particularly in the synthesis of complex molecules and natural products. Due to its spirocyclic structure, Spiro[4.5]decan-6-one offers opportunities for stereochemical control and the creation of chiral centers in target molecules. Its presence in the core structure of many biologically active compounds makes it a crucial intermediate for pharmaceutical research and drug development. Furthermore, the distinctive reactivity of Spiro[4.5]decan-6-one allows for the formation of diverse functional groups through various chemical transformations, making it a key player in the toolbox of synthetic chemists working towards the creation of novel molecules with specific properties and applications.