1574615-20-5

Basic information

• Product Name: (2S,3R,4R)-3-nitro-2-phenylthiochroman-4-ol
• Synonyms: (2S,3R,4R)-3-nitro-2-phenylthiochroman-4-ol
• CAS NO: 1574615-20-5
• Molecular Weight: 287.339
• Mol File: 1574615-20-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R)-3-nitro-2-phenylthiochroman-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R)-3-nitro-2-phenylthiochroman-4-ol(1574615-20-5)
• EPA Substance Registry System: (2S,3R,4R)-3-nitro-2-phenylthiochroman-4-ol(1574615-20-5)

Safety Data

• Hazardous Substances Data: 1574615-20-5(Hazardous Substances Data)

Upstream product

• 102-96-5 (2-nitroethenyl)benzene 
• 29199-11-9 2-formylthiophenol 
• 5153-67-3 nitrostyrene 

Downstream Products

• 1574616-17-3 (2S,3R,4R)-3-amino-2-phenylthiochroman-4-ol 

Relevant articles and documents

Chiral Bis(imidazolidine)iodobenzene (I-Bidine) Organocatalyst for Thiochromane Synthesis Using an Asymmetric Michael/Henry Reaction

Bis(imidazolidine)iodobenzene (I-Bidine) was designed as an organocatalyst based on previously reported imidazolidine- or oxazolidine-containing chiral metal catalysts. I-Bidine showed catalytic activity for the Michael/Henry reaction of thiosalicyl aldeh

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