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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-2-methanol, (2S)-

OC[C@H]1COC2(O1)CCCCC2 Request for Quotation
Chemical Name: 1,4-Dioxaspiro[4.5]decane-2-methanol, (2S)-
CAS Number: 95335-91-4
Product Number: AG003PWS(AGN-PC-0OO3AC)
Synonyms:
MDL No:
Molecular Formula: C9H16O3
Molecular Weight: 172.22154

Identification/Properties

Computed Properties
Molecular Weight:
172.224g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
172.11g/mol
Monoisotopic Mass:
172.11g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
152
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


D-α,β-Cyclohexylideneglycerol plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable tool in organic chemistry. This compound is commonly utilized in the formation of cyclic compounds, particularly in the synthesis of various heterocycles. Its cyclohexylidene group is essential for creating complex molecular architectures with high efficiency and selectivity. In addition, D-α,β-Cyclohexylideneglycerol is a key component in the preparation of chiral molecules, as its stereochemistry can be effectively harnessed to control the absolute configuration of the final products. Whether in the production of pharmaceuticals, agrochemicals, or advanced materials, the use of D-α,β-Cyclohexylideneglycerol in chemical synthesis enables chemists to access a wide array of structurally diverse and functionally-rich compounds with precision and reliability.