1256640-02-4

Basic information

• Product Name: C₂₉H₃₄O₆S
• Synonyms: C₂₉H₃₄O₆S
• CAS NO: 1256640-02-4
• Molecular Weight: 510.651
• Mol File: 1256640-02-4.mol

Chemical Properties

• CAS DataBase Reference: C₂₉H₃₄O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₉H₃₄O₆S(1256640-02-4)
• EPA Substance Registry System: C₂₉H₃₄O₆S(1256640-02-4)

Safety Data

• Hazardous Substances Data: 1256640-02-4(Hazardous Substances Data)

Upstream product

• 1256640-00-2 C₁₉H₂₂O₄ 
• 1256640-01-3 C₂₂H₂₈O₄ 
• 98-59-9 p-toluenesulfonyl chloride 
• 1256639-98-1 C₂₀H₂₂O₄ 
• 1256639-99-2 C₁₉H₂₂O₃ 
• 97-53-0 4-allylguaiacol 
• 16209-52-2 <4-(benzyloxy)-3-methoxyphenyl>acetaldehyde 
• 57371-42-3 4-allyl-1-benzyloxy-2-methoxybenzene 
• 100-39-0 benzyl bromide 

Downstream Products

• 1256640-03-5 C₂₉H₃₆O₈S 
• 1256640-04-6 C₂₈H₃₂O₇S 
• 1256640-05-7 C₂₈H₃₀O₆S 
• 1256640-06-8 C₂₁H₂₄O₆S 

Relevant articles and documents

A bismuth(III)-catalyzed friedel-crafts cyclization and stereocontrolled organocatalytic approach to (-)-platensimycin

A high yielding route to the (-)-platensimycin core is communicated. This entailed the discovery of Bi(OTf)3 to catalyze a Friedel-Crafts cyclization of a free lactol, supplemented by LiClO4 to suppress the Lewis basicity of the sulfonate group. After TBAF-promoted cyclodearomatization, a diastereoselective conjugate reduction of a dienone was achieved by adopting amine-based organocatalytic rationales to reverse the inherent steric control of the substrate.