42006-80-4

Basic information

• Product Name: (+/-)-formic acid-(1-methyl-2-phenyl-ethyl ester)
• Synonyms: (+/-)-formic acid-(1-methyl-2-phenyl-ethyl ester)
• CAS NO: 42006-80-4
• Molecular Weight: 164.204
• Mol File: 42006-80-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (+/-)-formic acid-(1-methyl-2-phenyl-ethyl ester)(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-formic acid-(1-methyl-2-phenyl-ethyl ester)(42006-80-4)
• EPA Substance Registry System: (+/-)-formic acid-(1-methyl-2-phenyl-ethyl ester)(42006-80-4)

Safety Data

• Hazardous Substances Data: 42006-80-4(Hazardous Substances Data)

Upstream product

• 300-57-2 allylbenzene 
• 64-18-6 formic acid 
• 65275-37-8 phenyl 2-phenylpropyl selenide 
• 68-12-2 N,N-dimethyl-formamide 
• 698-87-3 3-phenyl-2-propanol 
• 88959-00-6 2-phenylpropyl phenyl telluride 

Downstream Products

• 698-87-3 3-phenyl-2-propanol 

Relevant articles and documents

Silica triflate as an efficient reagent for the chemoselective formylation of alcohols

Silica triflate, as a new and stable silica-based reagent, is prepared by a reaction of silica gel with trifluoromethane sulfonyl chloride at room temperature. This reagent can be used for the efficient and selective formylation of alcohols in the presence of phenols in a relatively short reaction time and high yields under heterogeneous reaction conditions.

Mild and efficient procedure for acetylation and formylation of alcohols in the presence of Mg(HSO4)2

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Tf2O/Amide adducts: Versatile reagents for the synthesis of imidates and amidines

The Vilsmeier reagents generated from tertiary and secondary aliphatic and aromatic amides and trifluoromethanesulfonic anhydride (Tf2O) reacted with different nucleophiles (ROH, RSH, RNH2) affording the relative iminium and amidinium salts. The former, stable at room temperature, were easily transformed into the corresponding esters or O-alkyl thioesters by treatment with OH- or SH-.