370215
Methyl 3,5-dimethylbenzoate
98%
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About This Item
Produits recommandés
Niveau de qualité
Pureté
98%
Forme
solid
Point d'ébullition
239-240 °C (lit.)
Pf
31-33 °C (lit.)
Densité
1.027 g/mL at 25 °C (lit.)
Chaîne SMILES
COC(=O)c1cc(C)cc(C)c1
InChI
1S/C10H12O2/c1-7-4-8(2)6-9(5-7)10(11)12-3/h4-6H,1-3H3
Clé InChI
PEVXENGLERTHJE-UHFFFAOYSA-N
Catégories apparentées
Description générale
Methyl 3,5-dimethylbenzoate is an aromatic carboxylic acid ester. It was selected as ligand during monomer screening for the synthesis and investigation of various europium compounds containing pinacolyl methylphosphonate with different ligands. Methyl 3,5-dimethylbenzoate is reported as precursor of methyl-3,5-divinylbenzoate.
Application
Methyl 3,5-dimethylbenzoate may be used in the preparation of four carbon isostere related to highly active 4-pyridinemethanols, which were subsequently evaluated for their antimalarial activity. It may be used in the total synthesis of (±)-indoxamycin B.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
224.6 °F - closed cup
Point d'éclair (°C)
107.00 °C - closed cup
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Angewandte Chemie (International ed. in English), 51(14), 3474-3477 (2012-02-22)
Revised version: the first total synthesis of indoxamycin B leads to a stereochemical reassignment of the natural product. The synthetic route features an efficient carboannulation sequence to rapidly access the dihydroindenone system. Moreover, a series of Au(I)-catalyzed transformations served in
Molecularly imprinted polymers for the selective sequestering and sensing of ions.
The Johns Hopkins Medical Letter Health After 50, 18(4), 465-465 (1997)
Journal of medicinal chemistry, 23(11), 1198-1201 (1980-11-01)
Four carbon isosteres related to the highly active 4-pyridylcarbinolamines were prepared and evaluated for suppressive antimalarial activity against Plasmodium berghei in mice. Three of the four examples possessed significant activity but were approximately one dose level less active than the
Analytical chemistry, 71(2), 373-378 (1999-02-09)
The techniques of molecular imprinting and sensitized lanthanide luminescence have been combined to create the basis for a sensor that can selectively measure the hydrolysis product of the nerve agent Soman in water. The sensor functions by selectively and reversibly
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