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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)-

Benzenemethanol, a-2-propenyl-

C=CCC(c1ccccc1)O Request for Quotation
Chemical Name: Benzenemethanol, a-2-propenyl-
CAS Number: 936-58-3
Product Number: AG003EM6(AGN-PC-0W3A5R)
Synonyms:
MDL No:
Molecular Formula: C10H12O
Molecular Weight: 148.2017

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
148.205g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
148.089g/mol
Monoisotopic Mass:
148.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
114
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Phenyl-3-buten-1-ol is a versatile compound commonly utilized in chemical synthesis due to its unique reactivity and functionality. This compound, also known as β-hydroxy styrene, serves as a valuable building block in organic chemistry, offering a wide range of applications in the synthesis of various important chemicals and pharmaceuticals.One of the key applications of 1-Phenyl-3-buten-1-ol lies in its role as a precursor for the synthesis of chiral molecules. Its chiral center allows for the creation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of new drugs with enhanced efficacy and reduced side effects. By utilizing 1-Phenyl-3-buten-1-ol as a starting material, chemists can access a diverse array of chiral products through selective transformations and functional group manipulations.Moreover, 1-Phenyl-3-buten-1-ol can also be employed in the synthesis of various fine chemicals and natural products. Its unique structure enables the construction of complex molecular scaffolds through strategic bond-forming reactions, making it a valuable reagent in the preparation of specialty chemicals, flavors, fragrances, and other high-value compounds.Overall, the versatility and reactivity of 1-Phenyl-3-buten-1-ol make it a valuable tool in chemical synthesis, allowing for the efficient and selective construction of diverse organic molecules with important applications in pharmaceuticals, agrochemicals, and materials science.