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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)-

1,3-Dioxolane, 4-methyl-2-pentyl-

CCCCCC1OCC(O1)C Request for Quotation
Chemical Name: 1,3-Dioxolane, 4-methyl-2-pentyl-
CAS Number: 1599-49-1
Product Number: AG001RII(AGN-PC-0468OH)
Synonyms:
MDL No:
Molecular Formula: C9H18O2
Molecular Weight: 158.2380

Identification/Properties

Properties
BP:
186.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
1.4350 (estimate)
Computed Properties
Molecular Weight:
158.241g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
158.131g/mol
Monoisotopic Mass:
158.131g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
104
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-2-pentyl-1,3-dioxolane is a versatile compound that finds extensive application in organic chemical synthesis. This cyclic acetal is commonly used as a protecting group for sensitive ketone functionalities during multi-step organic reactions. By selectively masking the ketone group with 4-Methyl-2-pentyl-1,3-dioxolane, unwanted side reactions or undesired interactions with other reagents can be avoided, allowing for targeted transformations at specific functional groups. This protective strategy enables chemists to control the regioselectivity and stereochemistry of complex molecular structures, facilitating the synthesis of a wide range of organic compounds with high precision and efficiency. Additionally, 4-Methyl-2-pentyl-1,3-dioxolane can serve as a stable precursor for the introduction of ketone functionality in organic molecules, providing a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its compatibility with a variety of reagents and reaction conditions makes it a valuable tool for synthetic chemists seeking to optimize synthetic routes and streamline chemical transformations in their research and development projects.