Dimethyl 5-hydroxyisophthalate
Dimethyl 5-hydroxyisophthalate undergoes a base-catalyzed nucleophilic oxirane ring-opening addition reaction with allyl glycidyl ether, to afford 5-substituted derivatives of isophthalic acid. Influence of third component, i. e. a series of 1,ω-alkanediols on the copolymerization reaction of dimethyl 5-hydroxyisophthalate with poly(ethylene glycol) has been studied. Lipase-catalyzed condensation polymerization of dimethyl 5-hydroxyisophthalate with polyethylene glycol is reported.
Catalog Number | CBB1115080 |
Alternative Name(s) | Dimethyl 5-hydroxybenzene-1,3-dicarboxylate |
Molecular Formula | HOC6H3-1,3-(CO2CH3)2 |
CAS# | 13036-02-7 |
Purity | >98% |
Inchi | 1S/C10H10O5/c1-14-9(12)6-3-7(10(13)15-2)5-8(11)4-6/h3-5,11H,1-2H3 |
Inchi Key | DOSDTCPDBPRFHQ-UHFFFAOYSA-N |
SMILES | COC(=O)c1cc(O)cc(c1)C(=O)OC |
Size | Inquiry |
Supplier Page | https://www.amerigoscientific.com/dimethyl-5-hydroxyisophthalate-item-115080.html |