26549-63-3

Basic information

• Product Name: trans-1,2-dihydrophthalic acid dimethyl ester
• CAS NO: 26549-63-3
• Molecular Weight: 196.203
• Mol File: 26549-63-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: trans-1,2-dihydrophthalic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: trans-1,2-dihydrophthalic acid dimethyl ester(26549-63-3)
• EPA Substance Registry System: trans-1,2-dihydrophthalic acid dimethyl ester(26549-63-3)

Safety Data

• Hazardous Substances Data: 26549-63-3(Hazardous Substances Data)

Upstream product

• 5675-13-8 trans-cyclohexa-3,5-diene-1,2-dicarboxylic acid 
• 2409-87-2 methyl (2E)-penta-2,4-dienoate 
• 186581-53-3 diazomethane 
• 26554-23-4 1,3-Cyclohexadien-r-5,c-6-dicarbonsaeure 
• 108-24-7 acetic anhydride 
• 67-56-1 methanol 
• 1515-19-1 cis-cyclohexa-3,5-diene-1,2-dicarboxylic anhydride 

Downstream Products

• 118215-79-5 (1S,2R,3R,4R,7R,8S)-7,8-Bis-benzenesulfonyl-bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic acid dimethyl ester 
• 118215-79-5 (1R,2S,3S,4S,7R,8R)-7,8-Bis-benzenesulfonyl-bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic acid dimethyl ester 
• 51698-72-7 C₂₄H₂₆O₆S₂ 
• 65-85-0 benzoic acid 
• 84-66-2 Diethyl phthalate 
• 19926-49-9 2-phenylbenzoic acid ethyl ester 
• 131-11-3 phthalic acid dimethyl ester 
• 77803-95-3 r-1-Acetamido-c-2,c-3,c-4-trisacetoxycyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-95-3 r-1-Acetamido-t-2,t-3,c-4-triacetoxy-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-95-3 r-1-Acetamido-c-2,t-3,c-4-trisacetoxycyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-97-5 r-1-Acetamido-c-2,c-4-diacetoxy-t-3-bromcyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-93-1 r-1-Acetamido-c-4-acetoxy-2-cyclohexen-t-5,t-6-dicarbonsaeure-dimethylester 

Relevant articles and documents

Synthese de phosphinites derives de sucres: applications en cyclodimerisation du penta 2,4-dienoate de methyle, en hydrogenation et en hydrosilylation de la pentolactone

Sugar-derived phosphinites, when used as ligands in the catalytic hydrogenation of α-ketopentolactone, lead to the corresponding alcohol with a better enantiomeric excess (20percent) than in hydrosilylation (10percent).In the cyclodimerisation of penta-2,4-dienoic acid methyl ester they lead to the meso cycloocta-3,7-diene-1,2-doic dimethyl ester.

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, V. 1,3-Cyclohexadiene-5,6-dicarboxylic Acid Derivatives as Reactants

The use of 1,3-cyclohexadiene-5,6-dicarboxylic acid derivatives as educts for the reaction sequence: Diels-Alder reaction with nitroso compounds, reduction of the adducts, hydroxylation, gives hexa-substituted cyclohexanes.However, attempts to synthesize