1574615-43-2

Basic information

• Product Name: (2S,3R,4R)-2-(4-methoxyphenyl)-3-nitrothiochroman-4-ol
• Synonyms: (2S,3R,4R)-2-(4-methoxyphenyl)-3-nitrothiochroman-4-ol
• CAS NO: 1574615-43-2
• Molecular Weight: 317.365
• Mol File: 1574615-43-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R)-2-(4-methoxyphenyl)-3-nitrothiochroman-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R)-2-(4-methoxyphenyl)-3-nitrothiochroman-4-ol(1574615-43-2)
• EPA Substance Registry System: (2S,3R,4R)-2-(4-methoxyphenyl)-3-nitrothiochroman-4-ol(1574615-43-2)

Safety Data

• Hazardous Substances Data: 1574615-43-2(Hazardous Substances Data)

Upstream product

• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 29199-11-9 2-formylthiophenol 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 

Relevant articles and documents

Optically active thiochroman derivative and its manufacturing method

PROBLEM TO BE SOLVED: To establish a means of synthesizing a thiochroman derivative.SOLUTION: Provided is a thiochroman derivative represented by formula (2) (where, Rand Rmay respectively independently use H, Me, Et, tBu, halogen, alkoxy and a nitro group; and Rand Rmay be plurally coupled at any position).

Diversity-oriented asymmetric catalysis (DOAC): Stereochemically divergent synthesis of thiochromanes using an imidazoline-aminophenol-nickel-catalyzed michael/henry reaction

The (S,S)-diphenylethylenediamine-derived imidazoline-aminophenol-Ni complex catalyzed tandem asymmetric Michael/Henry reaction of 2-mercaptobenzaldehydes with β-nitrostyrenes to give the corresponding (2S,3R,4R)-2-aryl-3-nitrothiochroman-4-ols in up to 9