Chloroxylenol

(4-Chloro-1，2-Phenylene)Dimethanol.

Application (4-Chlorophenyl)triethoxysilane can be used: To facilitate the connection between dipolar mixed monolayers and&nbspzinc oxide in photovoltaic devices. As a substrate in the Ni-catalyzed decarboxylative coupling with alkynyl carboxylic

Application (4-Chlorophenyl)triethoxysilane can be used: To facilitate the connection between dipolar mixed monolayers and&nbspzinc oxide in photovoltaic devices. As a substrate in the Ni-catalyzed decarboxylative coupling with alkynyl carboxylic

(4R)-4-(2-Chlorophenyl)-2-hydroxy-5， 5-dimethyl-1， 3， 2-dioxaphosphinane 2-oxide.

(4R)-4-(2-Chlorophenyl)-2-hydroxy-5， 5-dimethyl-1， 3， 2-dioxaphosphinane 2-oxide.

(4R)-4-(2-Chlorophenyl)-2-hydroxy-5， 5-dimethyl-1， 3， 2-dioxaphosphinane 2-oxide.

(R)-(-)-2-Chloro-1-phenylethanol

( R )-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

( R )-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

( S )-(-)-1-Phenylethanol can be prepared from acetophenone via bioreduction in the presence of Rhizopus arrhizus as a biocatalyst.

( S )-(-)-1-Phenylethanol can be prepared from acetophenone via bioreduction in the presence of Rhizopus arrhizus as a biocatalyst.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.