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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-Dioxane, 5-(2-bromoethyl)-2,2-dimethyl-

BrCCC1COC(OC1)(C)C Request for Quotation
Chemical Name: 1,3-Dioxane, 5-(2-bromoethyl)-2,2-dimethyl-
CAS Number: 97845-58-4
Product Number: AG00H7E5(AGN-PC-0JNF6B)
Synonyms:
MDL No:
Molecular Formula: C8H15BrO2
Molecular Weight: 223.1075

Identification/Properties

Properties
BP:
239.2°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Liquid
Computed Properties
Molecular Weight:
223.11g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
222.026g/mol
Monoisotopic Mass:
222.026g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
115
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 5-(2-Bromoethyl)-2,2-dimethyl-1,3-dioxane is a versatile building block in chemical synthesis, commonly used for the introduction of a 2-bromoethyl functionality in organic molecules. This compound can be employed as a precursor for the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials.In organic synthesis, 5-(2-Bromoethyl)-2,2-dimethyl-1,3-dioxane can serve as a starting material for the preparation of diverse heterocyclic compounds through cyclization reactions. The presence of the bromoethyl group enables further functionalization via cross-coupling reactions, nucleophilic substitution, or palladium-catalyzed transformations.Additionally, this compound is utilized in the construction of complex molecular architectures due to its high reactivity and compatibility with a wide range of synthetic methodologies. Its unique structure and reactivity make it a valuable tool for accessing novel chemical entities with diverse properties and functionalities.In summary, the application of 5-(2-Bromoethyl)-2,2-dimethyl-1,3-dioxane in chemical synthesis offers a strategic approach for the design and synthesis of molecular scaffolds with potential applications in various fields of chemistry and beyond.