1. Home
  2. Oxiranemethanol, 3-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Oxiranemethanol, 3-phenyl-

OCC1OC1c1ccccc1 Request for Quotation
Chemical Name: Oxiranemethanol, 3-phenyl-
CAS Number: 21915-53-7
Product Number: AG006YLO(AGN-PC-0JLY30)
Synonyms:
MDL No:
Molecular Formula: C9H10O2
Molecular Weight: 150.1745

Identification/Properties

Computed Properties
Molecular Weight:
150.177g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
150.068g/mol
Monoisotopic Mass:
150.068g/mol
Topological Polar Surface Area:
32.8A^2
Heavy Atom Count:
11
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

Request for Quotation

Customer Feedback

Chemical Structure


The compound (3-Phenyloxiran-2-yl)methanol, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique molecular structure. Through its reactive epoxide functional group and hydroxyl moiety, $name$ can participate in a variety of synthetic transformations, making it a valuable intermediate in the creation of complex organic molecules.Its epoxide ring can undergo ring-opening reactions with nucleophiles, such as amines or thiols, leading to the formation of new carbon-carbon or carbon-heteroatom bonds. This reactivity allows for the incorporation of diverse functional groups into the molecule, expanding its synthetic utility.Furthermore, the hydroxyl group in $name$ provides opportunities for further derivatization, including esterification, etherification, or oxidation reactions. These modifications can tailor the compound's properties and enable the synthesis of specialized compounds for various applications in pharmaceuticals, agrochemicals, materials science, and other fields.Overall, the strategic placement of functional groups in (3-Phenyloxiran-2-yl)methanol offers chemists a valuable platform for designing and synthesizing novel compounds with enhanced properties and functionalities.