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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)-

(2R)-2-[(2-propan-2-ylphenoxy)methyl]oxirane

CC(c1ccccc1OCC1CO1)C Request for Quotation
Chemical Name: (2R)-2-[(2-propan-2-ylphenoxy)methyl]oxirane
CAS Number: 5904-89-2
Product Number: AG00EIU5(AGN-PC-0OCU1G)
Synonyms:
MDL No:
Molecular Formula: C12H16O2
Molecular Weight: 192.2542

Identification/Properties

Computed Properties
Molecular Weight:
192.258g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
192.115g/mol
Monoisotopic Mass:
192.115g/mol
Topological Polar Surface Area:
21.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
179
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-[(2-Isopropylphenoxy)methyl]oxirane, also known as $name$, plays a crucial role in chemical synthesis as a versatile organic compound. It is commonly utilized as a building block in the creation of various polymers, pharmaceuticals, and agrochemicals. The epoxide functionality of $name$ enables it to participate in different reactions, such as ring-opening reactions and cross-linking reactions, making it a valuable ingredient in the production of specialty chemicals. Its unique structure allows for modifications and substitutions, resulting in the generation of a wide range of derivatives with diverse properties and applications in the field of organic synthesis.