Dimethyl succinylo succinate

CAS : 6289-46-9

Ref. 3D-FD143929

Informations sur le produit

• Nom: Dimethyl succinylo succinate
• Synonymes: 1,4-Cyclohexanedicarboxylic acid, 2,5-dioxo-, 1,4-dimethyl ester, 1,4-Cyclohexanedicarboxylic acid, 2,5-dioxo-, dimethyl ester, 1,4-Dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate, 2,5-Dioxo-1,4-Cyclohexanedicarboxylic Acid Dimethyl Ester, Dimethyl 2,5-Dioxocyclohexane-1,4-Dicarboxylate, Dimethyl 2,5-dioxocyclohexane-1,4-carboxylate, Dimethyl cyclohexane-2,5-dione-1,4-dicarboxylate, Dimethyl succinosuccinate, Dimethyl succinylosuccinate, Dimethyl succinylsuccinate, Dmss, NSC 122567, NSC 5670, Succinosuccinic acid dimethyl ester, dimethyl (1R,4R)-2,5-dioxocyclohexane-1,4-dicarboxylate, dimethyl (1R,4S)-2,5-dioxocyclohexane-1,4-dicarboxylate, dimethyl (1S,4S)-2,5-dioxocyclohexane-1,4-dicarboxylate

Description

Dimethyl succinylo succinate is an experimental solubility data that has been studied by gravimetric analysis and ethyl formate. It is soluble in hydrochloric acid, dimethyl, and transport properties. The synthetic process of this compound is not clear. Phenyl groups are the most common substituents on this molecule. Dimethyl succinylo succinate has a molecular weight of 168.18 g/mol and a melting point of -14°C. The nmr spectra show the presence of two methyl groups with a methoxy group on the 2-carbon position on the phenyl ring. The reaction yield for this chemical is 50%. This chemical does not dissolve in water but does dissolve in calcium carbonate, which is used to manufacture cement for construction purposes.br>br>
Dimethyl succinylo succinate is used as a building material in construction due to its low cost, high strength, and resistance to heat and corrosion. It also provides protection

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 228.2 g/mol
• Formule: C₁₀H₁₂O₆
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C10H12O6/c1-15-9(13)5-3-8(12)6(4-7(5)11)10(14)16-2/h5-6H,3-4H2,1-2H3
• Code InChI: InChIKey=MHKKFFHWMKEBDW-UHFFFAOYSA-N
• SMILES: COC(=O)C1CC(=O)C(C(=O)OC)CC1=O