37729-18-3

Usage

Uses

Used in Industrial and Agricultural Applications:
Biphenyl-4-Ethanol is used as a germicide and fungicide for its ability to prevent microbial growth, making it suitable for various industrial and agricultural uses where controlling microbial contamination is essential.
Used in Food and Personal Care Products:
In the food industry, Biphenyl-4-Ethanol is used as a preservative to extend the shelf life of products by inhibiting the growth of spoilage-causing microorganisms. Similarly, in personal care products, it serves as a preservative to prevent microbial contamination and ensure product safety.
Used in Synthesis of Organic Compounds:
Biphenyl-4-Ethanol is utilized as a key intermediate in the synthesis of other organic compounds, contributing to the development of various chemical products and materials.
Used as a Corrosion Inhibitor in the Metalworking Industry:
In the metalworking industry, Biphenyl-4-Ethanol is employed as a corrosion inhibitor to protect metal surfaces from degradation and extend the life of equipment and structures.

Upstream product

• 2350-89-2 p-vinylbiphenyl 

Downstream Products

• 37729-59-2 Bis-(2-p-biphenylylethyl)-sulfit 
• 362476-92-4 (3-benzyloxycarbamoyl-3,4-dihydro-1H-isoquinolin-2-yl)-(4-methoxy-phenyl)-phosphinic acid 2-biphenyl-4-yl-ethyl ester 
• 913816-33-8 2-p-biphenylethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 913816-37-2 2-p-biphenylethyl 2-acetamido-2-deoxy-β-D-glucopyranoside 
• 913816-41-8 2-p-biphenylethyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 876913-98-3 4-(2-(4-nitrophenoxy)ethyl)biphenyl 
• 876914-62-4 4-[2-(2-methyl-4-nitro-phenoxy)-ethyl]biphenyl 
• 876914-61-3 4-[2-(2-chloro-4-nitro-phenoxy)-ethyl]biphenyl 
• 2350-89-2 p-vinylbiphenyl 

Relevant academic research and scientific papers

Enantioselective hydrosilylation of aromatic alkenes catalyzed by chiral bis(oxazolinyl)phenyl-rhodium acetate complexes

Highly efficient and enantioselective hydrosilylation of aromatic alkenes catalyzed by the chiral rhodium acetate complexes with the bis(oxazolinyl)phenyl ligands has been reported that afforded chiral silane derivatives with up to 99% ee. Georg Thieme Ve

Asymmetric hydrosilylation of alkenes with alkoxyhydrosilanes catalyzed by chiral bis(oxazolinyl)phenyl-rhodium complex

Asymmetric addition of alkoxyhydrosilanes to styrene derivatives was examined with chiral bis(oxazolinyl)phenyl-rhodium complex to give moderate ratios (up to 77:23) of α- and β-adducts and high enantioselectivity (up to 95% for the α-adduct).