1829-60-3

Basic information

• Product Name: Dimethyl 7-Oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate
• Synonyms: Dimethyl 7-Oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate
• CAS NO: 1829-60-3
• Molecular Formula: C₁₀H₁₀O₅
• Molecular Weight: 210.1834
• EINECS: -0
• Mol File: 1829-60-3.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 120°C/0.5mmHg(lit.)
• Appearance: /
• Refractive Index: 1.4940 to 1.4980
• CAS DataBase Reference: Dimethyl 7-Oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Dimethyl 7-Oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate(1829-60-3)
• EPA Substance Registry System: Dimethyl 7-Oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate(1829-60-3)

Safety Data

• Hazardous Substances Data: 1829-60-3(Hazardous Substances Data)

Upstream product

• 625-86-5 2,5-dimethylfuran 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 110-00-9 furan 
• 51153-59-4 1,4-Dioxocin 

Downstream Products

• 51720-14-0 dimethyl 1-(2-ethoxy-2-oxoethyl)-1H-1,2,3-triazole-4,5-dicarboxylate 
• 4314-21-0 ethyl 2-(1H-1,2,3-triazol-1-yl)acetate 
• 38791-02-5 isoxazol-3-yl(phenyl)methanone 
• 4282-33-1 dimethyl 3,4-furandicarboxylate 
• 79379-93-4 3-benzoyl-4,5-isoxazoledicarboxylic acid dimethyl ester 
• 126690-96-8 9-bromodibenzobarrelene 
• 135505-83-8 Mo(CHC₄H₂O(COOCH₃)2)(CHCHC(CH₃)2(C₆H₅))(NC₆H₃(CH(CH₃)2)2)(OC(CH₂CH₃)3)2 
• 1198182-83-0 dimethyl 6-hydroxy-1-methylcyclohexa-2,4-diene-1,2-dicarboxylate 
• 1198182-86-3 dimethyl 1-ethyl-6-hydroxycyclohexa-2,4-diene-1,2-dicarboxylate 
• 1198182-89-6 dimethyl 6-hydroxy-1-isobutylcyclohexa-2,4-diene-1,2-dicarboxylate 
• 1198182-88-5 dimethyl 1-butyl-6-hydroxycyclohexa-2,4-diene-1,2-dicarboxylate 

Relevant articles and documents

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NBE-Controlled Palladium-Catalyzed Interannular Selective C-H Silylation: Access to Divergent Silicon-Containing 1,1′-Biaryl-2-Acetamides

A novel palladium-catalyzed interannular selective C-H silylation of 1,1′-biaryl-2-acetamides is described. The combination of palladium catalyst with copper oxidant enables meta- or ortho-selective C-H silylation by employing hexamethyldisilane as a trimethylsilyl source, which relies on the control of NBE derivatives as a switch, thus providing straightforward access to divergent silicon-containing 1,1′-biaryl-2-acetamides.

METHOD TO PREPARE PHENOLICS FROM BIOMASS

The present invention is directed to a method for preparing a final phenolic product from biomass comprising the steps of providing a furanic compound obtainable from biomass; reacting the furanic compound with a dienophile to obtain a phenolic compound; reacting the phenolic compound further to obtain the final phenolic product.