77106-50-4

Basic information

• Product Name: Benzene, 1,2-dimethoxy-4-(1-methylethoxy)-
• Synonyms: Benzene, 1,2-dimethoxy-4-(1-methylethoxy)-
• CAS NO: 77106-50-4
• Molecular Formula: C₁₁H₁₆O₃
• Molecular Weight: 196.24
• Mol File: 77106-50-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 268.4°C at 760 mmHg
• Flash Point: 88.5°C
• Appearance: /
• Density: 1.007g/cm³
• Vapor Pressure: 0.0127mmHg at 25°C
• Refractive Index: 1.481
• CAS DataBase Reference: Benzene, 1,2-dimethoxy-4-(1-methylethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2-dimethoxy-4-(1-methylethoxy)-(77106-50-4)
• EPA Substance Registry System: Benzene, 1,2-dimethoxy-4-(1-methylethoxy)-(77106-50-4)

Safety Data

• Hazardous Substances Data: 77106-50-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H16O3/c1-8(2)14-9-5-6-10(12-3)11(7-9)13-4/h5-8H,1-4H3

Upstream product

• 93-07-2 Veratric acid 
• 75-30-9 2-iodo-propane 
• 2033-89-8 3,4-dimethoxyphenol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 75-26-3 isopropyl bromide 

Downstream Products

• 181423-71-2 14-(3,4-dimethoxyphenyl)-2,3,11,12-tetramethoxy-8,9-dihydro-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one 
• 96410-35-4 2',5,7-triisopropyloxy-4',5',6-trimethoxyflavone 
• 96410-34-3 2'-hydroxy-2,4',6'-triisopropyloxy-4,5,5'-trimethoxychalcone 
• 96410-36-5 2',5,7-trihydroxy-4',5',6-trimethoxyflavone 
• 96501-85-8 4,5-dimethoxy-2-isopropoxybenzene-1-carboaldehyde 
• 244160-46-1 1-bromo-4,5-dimethoxy-2-(propan-2-yloxy)benzene 

Relevant articles and documents

First total synthesis of medicinally important 3,4,7-trimethoxy-9,10-dihydrophenanthrene-1,5-diol

The first total synthesis was successfully achieved for biologically active 9,10-dihydrophenanthrene-1,5-diol. The key features of our synthetic approach are Perkin condensation, followed by bromination, palladium mediated intramolecular C-C bond coupling, and selective isopropyl ether cleavage. Synthesized compounds were purified and characterized by IR, 1HNMR, 13CNMR and HRMS/LC-MS.

Synthetic studies on flavone derivatives. XIV. Synthesis of 2',4'-5'-trioxygenated flavones

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