Dimenoxadol

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

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

Dimethyl Diglycolate.

Dimethyl Diglycolate.

Dimethyl Diglycolate.

Dimethyl Isopropylmalonate.

Dimethyl malonate undergoes enantioselective palladium-catalyzed allylic substitution reaction with 1,3-diphenylprop-2-enyl acetate to yield diastereomeric pure thienylpyridines . Application Dimethyl malonate was used in gold catalyzed oxidative

Synonym(s): Naphthalene-2,6-dicarboxylic acid dimethyl ester Formula: C14H12O4 Formula weight: 244.25 Purity: 99+% CAS Number: 840-65-3 Harmonized Tariff Code:  2917.39

General description Dimethyl succinate can be used as a flavoring agent in the food industry.

General description Dimethyl succinate can be used as a flavoring agent in the food industry.

Dimethyl Sulfoxide is an apolar protic solvent that is generally used as a reaction medium and reagent in organic reactions. Application Dimethyl Sulfoxide may be used as an oxidant for the conversion of isonitriles into isocyanates.

Dimethyl Sulfoxide is an apolar protic solvent that is generally used as a reaction medium and reagent in organic reactions. Application Dimethyl Sulfoxide may be used as an oxidant for the conversion of isonitriles into isocyanates.