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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)-

2-Propen-1-ol, 3-phenyl-, acetate

CC(=O)OC/C=C/c1ccccc1 Request for Quotation
Chemical Name: 2-Propen-1-ol, 3-phenyl-, acetate
CAS Number: 103-54-8
Product Number: AG00H9WP(AGN-PC-0JDZVS)
Synonyms:
MDL No:
Molecular Formula: C11H12O2
Molecular Weight: 176.2118

Identification/Properties

Computed Properties
Molecular Weight:
176.215g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
176.084g/mol
Monoisotopic Mass:
176.084g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Propen-1-ol, 3-phenyl-, 1-acetate is a versatile compound widely used in chemical synthesis. As an important building block in organic chemistry, this compound serves as a key intermediate in the preparation of various fine chemicals and pharmaceuticals. Its acetoxy group enhances its reactivity, allowing for facile derivatization and subsequent incorporation into complex molecules. In particular, 2-Propen-1-ol, 3-phenyl-, 1-acetate is frequently employed in the synthesis of fragrances, flavors, and pharmaceuticals due to its ability to introduce the phenyl group into target molecules while maintaining overall structural integrity. Additionally, its presence can impart desirable aromatic or medicinal properties to the final products. This compound's reactivity and versatility make it a valuable tool for organic chemists seeking to create novel compounds with tailored functionalities.