1. Home
  2. Benzenemethanol, a-methyl-, acetate

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)-

Benzenemethanol, a-methyl-, acetate

CC(c1ccccc1)OC(=O)C Request for Quotation
Chemical Name: Benzenemethanol, a-methyl-, acetate
CAS Number: 93-92-5
Product Number: AG00IHG5(AGN-PC-0W3IYF)
Synonyms:
MDL No:
Molecular Formula: C10H12O2
Molecular Weight: 164.2011

Identification/Properties

Computed Properties
Molecular Weight:
164.204g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
164.084g/mol
Monoisotopic Mass:
164.084g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
148
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

Request for Quotation

Customer Feedback

Chemical Structure


1-Phenylethyl acetate, also known as phenethyl acetate, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the production of various fragrances and flavoring agents due to its pleasant floral and fruity odor. In the field of organic chemistry, 1-Phenylethyl acetate is commonly employed as an esterification reagent, facilitating the formation of esters through reaction with alcohols in the presence of an acid catalyst. This process is crucial for the synthesis of numerous aromatic compounds used in perfumery, cosmetics, and food industries. Additionally, 1-Phenylethyl acetate can be utilized in the creation of pharmaceutical intermediates, providing a strategic starting material for the synthesis of diverse drug molecules. Its unique chemical properties and versatile applications make 1-Phenylethyl acetate a valuable asset in the realm of chemical synthesis.