96909-75-0

Upstream product

• 1983-71-7 (+/-)-3,4-dihydro-2,5,7,8-tetramethyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-ol 
• 700-13-0 Trimethylhydroquinone 
• 163234-46-6 6-benzyloxy-2,5,7,8-tetramethyl-2-(4-methyl-pent-3-enyl)-chroman 
• 201230-82-2 carbon monoxide 

Downstream Products

• 933474-06-7 (2RS)-2-(3'-acetoxyprop-2'-en-1'-yl)-6-benzyloxy-2,5,7,8-tetramethylchroman 
• 53713-44-3 rac-3,4-dihydro-2,5,7,8-tetramethyl-6-(phenylmethoxy)-2H-1-benzopyran-2-acetaldehyde 
• 53713-38-5 rac-3,4-dihydro-2,5,7,8-tetramethyl-6-(phenylmethoxy)-2H-1-benzopyran-2-acetic acid 

Relevant academic research and scientific papers

Synthesis of α-tocopherol and naphthotocopherol analogs with a carboxyl group in the side chain

On the basis of ozonolysis of short-chain α-tocopherol and naphthotocopherol analogs with a terminal isopropylidene group in the side chain, a general approach to the synthesis of 6-hydroxy-2,5,7,8- tetrtamethylchroman-2-yl-and 6-hydroxy-2,5-dimethyl-3,4-

Bidentate ligands by self-assembly through hydrogen bonding: A general room temperature/ambient pressure regioselective hydroformylation of terminal alkenes

The 6-DPPon (1)/rhodium catalyst allows for the first time a room temperature/ambient pressure regioselective hydroformylation of terminal alkenes with low catalyst loadings in good activity. The generality of this catalyst under these conditions was demonstrated for a wide range of structurally diverse alkenes equipped with many important functional groups. Thus, this practical and highly selective hydroformylation protocol, which omits the need for special pressure equipment, should find wide application in organic synthesis.