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2-([1,1'-biphenyl]-4-yl)propan-1-ol, also known as 2-(4-phenylphenyl)propan-1-ol, is an organic compound with the molecular formula C15H16O. It is a colorless liquid at room temperature and has a molecular weight of 212.29 g/mol. 2-([1,1'-biphenyl]-4-yl)propan-1-ol is characterized by a propane-1-ol group (a three-carbon chain with a hydroxyl group at the end) and a 1,1'-biphenyl-4-yl group (a biphenyl ring system with a phenyl group attached at the 4-position). It is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural properties. The compound is typically synthesized through various chemical reactions, such as Friedel-Crafts alkylation or nucleophilic substitution, and is known for its stability and reactivity in organic synthesis.

6725-53-7

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6725-53-7 Usage

Physical appearance

White, crystalline powder.

Solubility

Insoluble in water, soluble in organic solvents.

Applications

Synthesis of pharmaceuticals and agrochemicals, production of flavor and fragrance compounds, manufacture of polymers and resins.

Chemical role

Acts as a chiral catalyst in various chemical reactions.

Industry relevance

Valuable ingredient in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6725-53-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6725-53:
(6*6)+(5*7)+(4*2)+(3*5)+(2*5)+(1*3)=107
107 % 10 = 7
So 6725-53-7 is a valid CAS Registry Number.

6725-53-7Downstream Products

6725-53-7Relevant academic research and scientific papers

Copper-catalyzed hydroformylation and hydroxymethylation of styrenes

Franke, Robert,Geng, Hui-Qing,Meyer, Tim,Wu, Xiao-Feng

, p. 14937 - 14943 (2021/12/02)

Hydroformylation catalyzed by transition metals is one of the most important homogeneously catalyzed reactions in industrial organic chemistry. Millions of tons of aldehydes and related chemicals are produced by this transformation annually. However, most of the applied procedures use rhodium catalysts. In the procedure described here, a copper-catalyzed hydroformylation of alkenes has been realized. Remarkably, by using a different copper precursor, the aldehydes obtained can be further hydrogenated to give the corresponding alcohols under the same conditions, formally named as hydroxymethylation of alkenes. Under pressure of syngas, various aldehydes and alcohols can be produced from alkenes with copper as the only catalyst, in excellent regioselectivity. Additionally, an all-carbon quaternary center containing ethers and formates can be synthesized as well with the addition of unactivated alkyl halides. A possible reaction pathway is proposed based on our results. This journal is

Iron-Catalyzed Borrowing Hydrogen β- C(sp3)-Methylation of Alcohols

Polidano, Kurt,Williams, Jonathan M. J.,Morrill, Louis C.

, p. 8575 - 8580 (2019/09/12)

Herein we report the iron-catalyzed β-C(sp3)-methylation of primary alcohols using methanol as a C1 building block. This borrowing hydrogen approach employs a well-defined bench-stable (cyclopentadienone)iron(0) carbonyl complex as precatalyst (5 mol %) and enables a diverse selection of substituted 2-arylethanols to undergo β-C(sp3)-methylation in good isolated yields (24 examples, 65% average yield).

Practical synthesis of pharmaceutically relevant molecules enriched in sp3 character

Campbell, Peter S.,Jamieson, Craig,Simpson, Iain,Watson, Allan J. B.

, p. 46 - 49 (2017/12/27)

The expedient synthesis of compounds enriched in sp3 character is key goal in modern drug discovery. Herein, we report how a single pot Suzuki-Miyaura-hydrogenation can be used to furnish lead and fragment-like products in good to excellent yields. The approach has been successfully applied in formats amenable to parallel synthesis, in an asymmetric sense, and in the preparation of molecules with annotated biological activity.

Synthesis of alcohols via a rhodium-catalyzed hydroformylation-reduction sequence using tertiary bidentate amine ligands

Cheung, Lawrence L. W.,Vasapollo, Giuseppe,Alper, Howard

supporting information; experimental part, p. 2019 - 2022 (2012/09/22)

The synthesis of alcohols from aromatic olefins is described using a rhodium-catalyzed hydroformylation-reduction sequence with the assistance of a tertiary diamine ligand. The alcohols are produced in excellent branched to linear ratios and in good to excellent isolated yields. In all cases no aldehyde product, from hydroformylation, or alkyl product, from olefin reduction, was detected. Copyright

Bioconversion of aromatic compounds by Escherichia coli that expresses cytochrome P450 CYP153A13a gene isolated from an alkane-assimilating marine bacterium Alcanivorax borkumensis

Otomatsu, Toshihiko,Bai, Liming,Fujita, Naoya,Shindo, Kazutoshi,Shimizu, Keiko,Misawa, Norihiko

experimental part, p. 234 - 240 (2011/01/03)

The cytochrome P450 CYP153 family has been isolated from alkane-assimilating bacteria. CYP153 has been shown to mediate terminal hydroxylations of linear alkanes or alkyl aromatics. We here performed the biotransformation of various aromatic compounds by Escherichia coli cells that expressed the CYP153A13a (P450balk) gene, which was isolated from an alkane-degading marine bacterium Alcanivorax borkumensis. Aromatic compounds including a short alkyl moiety or methyl ether moiety, and phenolic compounds were converted to their respective hydroxylated products, whose structures were determined by HRMS and NMR analyses. The present study revealed that the catalytic function of CYP153A13a is multifunctional, i.e., it can hydroxylate not only the terminal of short alkyl groups that attached to aromatic rings but also the p-position of phenolic compounds substituted with a halogen or the acetyl group. CYP153A13a was also shown to demethylate methylether-including aromatic compounds.

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