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370215

Sigma-Aldrich

Methyl 3,5-dimethylbenzoate

98%

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5 G
CHF 25.10

CHF 25.10

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5 G
CHF 25.10

About This Item

Formula condensata:
(CH3)2C6H3CO2CH3
Numero CAS:
25081-39-4
Peso molecolare:
164.20
Numero MDL:
MFCD00077971
Codice UNSPSC:
12352100
ID PubChem:
24863065
NACRES:
NA.22

CHF 25.10

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Livello qualitativo

100

Saggio

98%

Stato

solid

P. ebollizione

239-240 °C (lit.)

Punto di fusione

31-33 °C (lit.)

Densità

1.027 g/mL at 25 °C (lit.)

Gruppo funzionale

ester

Stringa SMILE

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
PEVXENGLERTHJE-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

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.[1] Methyl 3,5-dimethylbenzoate is reported as precursor of methyl-3,5-divinylbenzoate.[2]

Applicazioni

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.[3] It may be used in the total synthesis of (±)-indoxamycin B.[4]

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

224.6 °F - closed cup

Punto d’infiammabilità (°C)

107.00 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
S43539
10109BE
S34174
15511BU
14123KG

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A Markovac et al.
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
Molecularly imprinted polymers for the selective sequestering and sensing of ions.
The Johns Hopkins Medical Letter Health After 50, 18(4), 465-465 (1997)
Oliver F Jeker et al.
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
A L Jenkins et al.
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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