18093-01-1

Basic information

• Product Name: 2,4-dimethoxyphenyl benzoate
• Synonyms: 2,4-dimethoxyphenyl benzoate
• CAS NO: 18093-01-1
• Molecular Weight: 258.274
• Mol File: 18093-01-1.mol

Chemical Properties

• CAS DataBase Reference: 2,4-dimethoxyphenyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dimethoxyphenyl benzoate(18093-01-1)
• EPA Substance Registry System: 2,4-dimethoxyphenyl benzoate(18093-01-1)

Safety Data

• Hazardous Substances Data: 18093-01-1(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 88874-66-2 2-Benzoyloxy-5-methoxy-phenol 
• 90264-46-3 4-benzoyloxy-resorcinol 
• 74-88-4 methyl iodide 
• 66417-42-3 (E)-3-(2,4-dimethoxy-phenyl)-acrylic acid methyl ester 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 150-19-6 O-methylresorcine 
• 150-76-5 4-methoxy-phenol 
• 94-36-0 dibenzoyl peroxide 
• 13330-65-9 2,4-dimethoxyphenol 
• 65-85-0 benzoic acid 

Downstream Products

• 65-85-0 benzoic acid 

Relevant articles and documents

Mechanically induced solvent-free esterification method at room temperature

Herein, we describe two novel strategies for the synthesis of esters, as achieved under high-speed ball-milling (HSBM) conditions at room temperature. In the presence of I2 and KH2PO2, the reactions afford the desired esterification derivatives in 45% to 91% yields within 20 min of grinding. Meanwhile, using KI and P(OEt)3, esterification products can be obtained in 24% to 85% yields after 60 min of grinding. In addition, the I2/KH2PO2 protocol was successfully extended to the late-stage diversification of natural products showing the robustness of this useful approach. Further application of this method in the synthesis of inositol nicotinate was also discussed. This journal is