Cyclofenil diphenol

2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following: . boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process . (2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with

2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following: . boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process . (2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with

2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following: . boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process . (2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with

Product description：Asymmetric reduction of 2,2,2-triphenylacetophenone using with potassium 9-O-(1,2: 5, 6-di-O-isopropylidene-α-D-glucofuranosyl)-9-boratabicyclo [3.3.1] nonane (chiral reducing agent) has been reported . Dehydrative cyclization of

Product description：Asymmetric reduction of 2,2,2-triphenylacetophenone using with potassium 9-O-(1,2: 5, 6-di-O-isopropylidene-α-D-glucofuranosyl)-9-boratabicyclo [3.3.1] nonane (chiral reducing agent) has been reported . Dehydrative cyclization of

Product description：Asymmetric reduction of 2,2,2-triphenylacetophenone using with potassium 9-O-(1,2: 5, 6-di-O-isopropylidene-α-D-glucofuranosyl)-9-boratabicyclo [3.3.1] nonane (chiral reducing agent) has been reported . Dehydrative cyclization of

Product description：Asymmetric reduction of 2,2,2-triphenylacetophenone using with potassium 9-O-(1,2: 5, 6-di-O-isopropylidene-α-D-glucofuranosyl)-9-boratabicyclo [3.3.1] nonane (chiral reducing agent) has been reported . Dehydrative cyclization of

2,2-Diphenylpropionitrile.

2,2-Diphenylpropionitrile.

2,2-Diphenylpropionitrile.

2,2-Diphenylpropionitrile.

CAS Number: 886-38-4 Solubility: (20&degC) insoluble Melting Point: 118 - 122&degC Molar Mass: 206.24 g/mol