57705-17-6

Basic information

• Product Name: ethyl 3,5-dimethyl-phenol-2-carboxylate
• Synonyms: ethyl 3,5-dimethyl-phenol-2-carboxylate
• CAS NO: 57705-17-6
• Molecular Weight: 194.23
• Mol File: 57705-17-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 3,5-dimethyl-phenol-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3,5-dimethyl-phenol-2-carboxylate(57705-17-6)
• EPA Substance Registry System: ethyl 3,5-dimethyl-phenol-2-carboxylate(57705-17-6)

Safety Data

• Hazardous Substances Data: 57705-17-6(Hazardous Substances Data)

Upstream product

• 1522-41-4 ethyl-2-fluoroacetoacetate 
• 3102-33-8 trans-3-penten-2-one 
• 33499-42-2 2,4-dimethylbenzoic acid ethyl ester 
• 25145-04-4 (Z)-4-trimethylsiloxypent-3-en-2-one 
• 89186-81-2 1-ethoxy-1,3-bis[(trimethylsilyl)oxy]buta-1,3-diene 
• 64-17-5 ethanol 
• 6370-32-7 2-hydroxy-4,6-dimethylbenzoic acid 

Downstream Products

• 947340-34-3 ethyl 2,4-dimethyl-6-(trifluoromethylsulfonyloxy)benzoate 

Relevant articles and documents

One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors

A new strategy for the synthesis of 3,5-disubstituted phenols is established through one-pot Robinson annulation of α,β-unsaturated ketones with α-fluoro-β-ketoesters followed by in situ dehydrofluorination and tautomerization. This method has been extended to the synthesis of polysubstituted phenols and applied in the preparation of biologically active compounds.

Synthesis of dibenzo[b,d]pyran-6-ones based on a '[3+3] cyclization-Suzuki cross-coupling' strategy

Functionalized dibenzo[b,d]pyran-6-ones were prepared by sequential '[3+3] cyclization-Suzuki cross-coupling' reactions.