1033366-39-0

Basic information

• Product Name: C₁₆H₁₃ClO₂
• Synonyms: C₁₆H₁₃ClO₂
• CAS NO: 1033366-39-0
• Molecular Weight: 272.731
• Mol File: 1033366-39-0.mol

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₃ClO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₃ClO₂(1033366-39-0)
• EPA Substance Registry System: C₁₆H₁₃ClO₂(1033366-39-0)

Safety Data

• Hazardous Substances Data: 1033366-39-0(Hazardous Substances Data)

Upstream product

• 545343-49-5 2-((tert-butyldimethylsilyl)oxy)-5-chlorobenzaldehyde 
• 1325228-83-8 (E)-2-(4-(5-chloro-2-hydroxyphenyl)but-3-enyl)phenol 
• 1033366-30-1 C₁₆H₁₃ClO₂ 

Relevant articles and documents

Dramatic base-oriented chemoselective tandem wacker cyclizations: Synthesis of bisbenzannelated spiroketals and 2-substituted chromans

A Pd(II)/Cu(II)-catalyzed chemoselective tandem aerobic cyclization of phenolic olefins leads to [5,6]-bisbenzannelated spiroketals or 2-substituted chromans, wherein it was interestingly found that the presence or absence of base could be responsible for the tunable selectivity. The [5,6]- bisbenzannelated spiroketals were achieved from tandem Wacker cyclization-aroxylation in moderate yields in the absence of base, and 2-substituted chromans were formed through base-mediated Pd(II)/Cu(II)-catalyzed tandem Wacker cyclization-Michael addition in good yields. Georg Thieme Verlag Stuttgart ? New York.

Gold-catalyzed double intramolecular alkyne hydroalkoxylation: Synthesis of the bisbenzannelated spiroketal core of rubromycins

The synthesis of the bisbenzannelated spiroketal core of natural bioactive rubromycins via a gold-catalyzed double intramolecular hydroalkoxylation was described. A comparative study on the formation of aliphatic and of aromatic spiroketals was also condu