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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)-

1,4-Dioxaspiro[4.5]decane

C1CCC2(CC1)OCCO2 Request for Quotation
Chemical Name: 1,4-Dioxaspiro[4.5]decane
CAS Number: 177-10-6
Product Number: AG00252Q(AGN-PC-0JK8UR)
Synonyms:
MDL No:
Molecular Formula: C8H14O2
Molecular Weight: 142.1956

Identification/Properties

Properties
MP:
176-180℃
BP:
184°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
n20/D 1.459(lit.)
Computed Properties
Molecular Weight:
142.198g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
142.099g/mol
Monoisotopic Mass:
142.099g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Dioxaspiro[4.5]decane serves as a valuable building block in chemical synthesis, offering a versatile platform for the creation of various chemical compounds. Its unique structure and reactivity make it particularly useful in the synthesis of complex molecules with diverse applications. The spirocyclic nature of 1,4-Dioxaspiro[4.5]decane imparts stability and rigidity, making it a favored scaffold for constructing pharmaceuticals, agrochemicals, and materials with specific properties. Additionally, its reactivity allows for functionalization at different positions, enabling tailored derivatization to achieve desired properties in target molecules. As a key player in the realm of organic synthesis, 1,4-Dioxaspiro[4.5]decane offers chemists a powerful tool to access a wide array of structurally diverse and functionally sophisticated compounds.