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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-ethenyl-, (aS)-

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Chemical Name: Benzenemethanol, a-ethenyl-, (aS)-
CAS Number: 104713-12-4
Product Number: AG003C85(AGN-PC-0OTRRU)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The (R)-1-Phenyl-2-propen-1-ol is a versatile compound often utilized in chemical synthesis due to its unique reactivity and structural properties. In organic synthesis, this compound serves as a valuable building block for the preparation of various pharmaceuticals, fragrances, and fine chemicals. Its chiral nature, with a stereocenter at the alpha carbon, makes it an ideal starting material for asymmetric synthesis, allowing for the creation of enantiopure products with high selectivity. Additionally, (R)-1-Phenyl-2-propen-1-ol can act as a precursor for the synthesis of biologically active compounds, such as chiral alcohols and amino alcohols, through various functional group transformations and synthetic pathways. Its broad application in chemical synthesis highlights its significance as a key intermediate in the production of diverse organic molecules with controlled stereochemistry and specific reactivity profiles.