Name: Dimethyl 5-hydroxyisophthalate (98%)
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- Overview
  - 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.
    
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- Properties
  - Categories
    
    Organic Building Blocks
    
    Alternative Name
    
    Dimethyl 5-hydroxybenzene-1,3-dicarboxylate
    
    CAS Number
    
    13036-02-7
    
    Molecular Formula
    
    HOC6H3-1,3-(CO2CH3)2
    
    Molecular Weight
    
    210.18
    
    Purity
    
    98%
    
    SMILES
    
    COC(=O)c1cc(O)cc(c1)C(=O)OC
    
    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
    
    MDL Number
    
    MFCD00134367
    
    Others
    
    SID 24863128
    
    Hazard Information
    
    Warning
    Combustible Solids
    
    Note
    
    Please note that Amerigo Scientific does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.
    
    * For Research Use Only.

Dimethyl 5-hydroxyisophthalate (98%)

Dimethyl 5-hydroxyisophthalate (98%)

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