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One example is the Suzuki reaction where, in the presence of a Pd(0) catalyst and base, phenylboronic acid and vinyl halides are coupled to produce phenyl alkenes. [7] This method was generalized to a route producing biaryls by coupling phenylboronic acid with aryl halides. C-C bond forming processes commonly use phenylboronic acid as a reagent.
4-Nonylphenylboronic acid is a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC 50 of 9.1nM, and 870x selectivity for FAAH over the related enzyme MAGL, which it inhibits with an IC 50 of 7900nM. [1]
4-Formylphenyl boronic acid crystallizes in colorless needles [2] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [4] and readily forms dimers and cyclic trimeric anhydrides, which complicate purification and tend to protodeboronize, a secondary reaction that occurs frequently in the Suzuki coupling, with ...
A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1] As a compound containing a carbon–boron bond, members of this class thus belong to the larger class of organoboranes.
6-chloronicotinic acid: 5326-23-8 C 6 H 4 N 4: tricyanoaminopropene: C 6 H 4 O 2: orthobenzoquinone: 583-63-1 parabenzoquinone quinone: 106-51-4 C 6 H 5 Br: bromobenzene: 108-86-1 C 6 H 5 CHO: benzaldehyde: 100-52-7 C 6 H 5 CH 2 OH: benzyl alcohol: 100-51-6 C 6 H 5 Cl: chlorobenzene: 108-90-7 C 6 H 5 COCl: benzoyl chloride: 98-88-4 C 6 H 5 COO ...
Aminonaphthalenesulfonic acids are compounds with the composition C 10 H 6 (NH 2)(SO 3 H), being derived from naphthalene (C 10 H 8) substituted by an amino and sulfonic acid groups. These compounds are colorless solids.
Pages in category "4-Hydroxyphenyl compounds" The following 155 pages are in this category, out of 155 total. ... 4-Hydroxymandelic acid; 4'-Hydroxynorendoxifen;
Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.