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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)-

Oxirane, [(1,1-dimethylethoxy)methyl]-, (2R)-

CC(OC[C@@H]1OC1)(C)C Request for Quotation
Chemical Name: Oxirane, [(1,1-dimethylethoxy)methyl]-, (2R)-
CAS Number: 130232-98-3
Product Number: AG000U6P(AGN-PC-0O0XRR)
Synonyms:
MDL No:
Molecular Formula: C7H14O2
Molecular Weight: 130.1849

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
130.187g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
130.099g/mol
Monoisotopic Mass:
130.099g/mol
Topological Polar Surface Area:
21.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
93.6
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


(2R)-2-(tert-Butoxymethyl)oxirane is a versatile compound commonly used in chemical synthesis for various applications. This chiral epoxide is particularly valued for its role in asymmetric synthesis, where it serves as a key building block for creating complex molecules with high stereochemical control. Due to its unique structure and reactivity, (2R)-2-(tert-Butoxymethyl)oxirane is employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo ring-opening reactions enables the introduction of functional groups at specific positions, allowing chemists to tailor the properties of the final product. In addition, the chirality of this compound plays a crucial role in determining the enantioselectivity of many reactions, making it a valuable tool for achieving desired stereochemistry in organic synthesis.