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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)-

3,5,8-Trioxabicyclo[5.1.0]octane, 4,4-dimethyl-

CC1(C)OCC2C(CO1)O2 Request for Quotation
Chemical Name: 3,5,8-Trioxabicyclo[5.1.0]octane, 4,4-dimethyl-
CAS Number: 57280-22-5
Product Number: AG00EB2I(AGN-PC-0NEPV6)
Synonyms:
MDL No:
Molecular Formula: C7H12O3
Molecular Weight: 144.1684

Identification/Properties

Properties
BP:
179°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
1.4560 to 1.4600
Computed Properties
Molecular Weight:
144.17g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
144.079g/mol
Monoisotopic Mass:
144.079g/mol
Topological Polar Surface Area:
31A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This unique molecule plays a crucial role as a building block in organic chemistry, particularly in the creation of intricate molecular structures. One of the key applications of 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane in chemical synthesis is as a bridging moiety in the construction of cyclic compounds. Its bicyclic structure provides a rigid framework that can be manipulated to form various functionalized derivatives. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, natural products, and materials with specific properties. Furthermore, 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane is often employed as a protecting group in organic synthesis. By selectively masking reactive sites within a molecule, this compound enables chemists to carry out complex reactions with precision, preventing unwanted side reactions and facilitating the synthesis of target compounds.In summary, the significance of 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane lies in its utility as a versatile building block and protecting group in chemical synthesis, contributing to the development of novel compounds and the advancement of diverse fields within the realm of chemistry.