CAS 1149-23-1

éster de Hantzsch

Descripción:

éster de Hantzsch, conocido químicamente como 1,3-dimetil-4-(2,6-dimetilfenilo)-1,4-dihidropiridina-3,5-dicarboxilato, es un compuesto sintético utilizado principalmente en química orgánica como un bloque de construcción versátil para varias reacciones, particularmente en la síntesis de moléculas biológicamente activas. Se caracteriza por su estructura de dihidropiridina, que presenta un sistema de anillos fusionados que contribuye a su reactividad. El compuesto es típicamente un sólido amarillo a naranja a temperatura ambiente y es soluble en disolventes orgánicos como etanol y diclorometano. éster de Hantzsch es notable por su papel en la reacción de Hantzsch, donde se forma a través de la condensación de aldehídos, amoníaco y β-cetoésteres, lo que lleva a la producción de dihidropiridinas. Este compuesto también es reconocido por su capacidad para actuar como agente reductor en varias transformaciones químicas, lo que lo hace valioso en la química orgánica sintética. Su estabilidad y reactividad lo convierten en un intermediario útil en el desarrollo de productos farmacéuticos y agroquímicos.

Fórmula: C₁₃H₁₉NO₄

InChI: InChI=1/C13H19NO4/c1-5-17-12(15)10-7-11(13(16)18-6-2)9(4)14-8(10)3/h14H,5-7H2,1-4H3

Clave InChI: InChIKey=LJXTYJXBORAIHX-UHFFFAOYSA-N

SMILES: C(OCC)(=O)C=1CC(C(OCC)=O)=C(C)NC1C

Sinónimos:

• 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester
• 1,4-Dihydro-3,5-dicarboxylic acid diethyl ester-2,6-dimethylpyridine
• 2,6-Dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester
• 2,6-Dimethyl-3,5-di(carboethoxy)-1,4-dihydropyridine
• 2,6-Dimethyl-3,5-dicarbethoxy-1,4-dihydropyridine
• 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridin
• 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine
• 3,5-Bis(ethoxycarbonyl)-1,4-dihydro-2,6-dimethylpyridine
• 3,5-Bis(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine
• 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine
• 3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine
• 3,5-Diethoxycarbonyl-1,4-dihydro-2,6-dimethylpyridine
• 3,5-Diethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine
• 3,5-Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
• 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester
• 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-, diethyl ester
• Diethone
• Diethyl 2,6-Dimethyl-1,4-Dihydropyridine-3,5-Dicarboxylate
• Diethyl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
• Diludin
• Diludine
• Ethidine
• Hantzsch ester
• Hantzsch's dihydropyridine
• NSC 120573
• NSC 3344
• Rr 116
• 5-pyridinedicarboxylicacid,1,4-dihydro-2,6-dimethyl-diethylester
• rr116
• AURORA 4780
• etidin
• hantzschester
• DIETHYL 2,6-DIMETHYL-1,4-DIHYDRO-3,5-PYRIDINEDICARBOXYLATE
• diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate
• DIETHYL 2,6-DIMETHYL-1,4-DIHYDROPYRIDINEDICARBOXYLATE
• RARECHEM AQ NN 0171
• hantzsch’sdihydropyridine
• Dihydropyridinum

Diethyl 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate

CAS: 1149-23-1

Fórmula: C₁₃H₁₉NO₄

Pureza: >98.0%(HPLC)(N)

Forma y color: Light yellow to Yellow to Green powder to crystal

Peso molecular: 253.30

Ref: 3B-D3775

Diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate, 98%

CAS: 1149-23-1

Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate is a hydrogen source in conjugate reduction and organocatalytic reductive amination. It is used as a hydrogen source in organocatalytic reductive amination and conjugate reduction. This Thermo Scientific Chemicals brand product was originall

Fórmula: C₁₃H₁₉NO₄

Pureza: 98%

Forma y color: Crystals or powder or crystalline powder, Pale yellow to yellow to green

Peso molecular: 253.30

Ref: 02-H55752

Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

CAS: 1149-23-1

Fórmula: C₁₃H₁₉NO₄

Pureza: 98%

Forma y color: Solid

Peso molecular: 253.2943

Ref: IN-DA0034PZ

Diethyl 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate

CAS: 1149-23-1

Diethyl 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate

Fórmula: C₁₃H₁₉NO₄

Pureza: 95%

Forma y color: Yellow to Yellow-Green Solid-Powder

Peso molecular: 253.29426

Ref: 54-OR350125

Diethyl 1.4-Dihydro-2.6-dimethyl-3.5-pyridinedicarboxylate

CAS: 1149-23-1

Fórmula: C₁₃H₁₉NO₄

Peso molecular: 253.29

Ref: BE-BePure-21800

Diethyl 1,4-dihydro-2,6-dimethyl-3-5-pyridinedicarboxylate

CAS: 1149-23-1

Fórmula: C₁₃H₁₉NO₄

Pureza: 95%

Forma y color: Solid

Peso molecular: 253.298

Ref: 10-F076860

Etidin

CAS: 1149-23-1

Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate

Fórmula: C₁₃H₁₉NO₄

Pureza: 97%

Peso molecular: 253.29

Ref: IN-DG14960

3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine

CAS: 1149-23-1

Applications 3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine is a dihydropyridine derivative that have been tested for antimicrobial activities.
References Murthy, Y.L.. et al.: Bioorg. Med. Chem. Lett., 22, 6016 (2012); Vaitkuviene, A., et al.: Pharmacol. Rep., 58, 551 (2006);

Fórmula: C₁₃H₁₉NO₄

Forma y color: Neat

Peso molecular: 253.29

Ref: TR-D431030

Diethone

CAS: 1149-23-1

Diethone is a chemical compound that has been found to have a variety of biological effects. It has been shown to inhibit the activity of enzymes, such as phospholipase A2, cyclooxygenase-1 and -2, lipoxygenase-1 and -2, and glutathione S-transferases. In addition, diethone inhibits the synthesis of prostaglandins and leukotrienes. Diethone also has various physiological functions in humans. It is an eye irritant that can cause conjunctivitis and corneal damage if it comes into contact with the eye. Diethone also inhibits toll-like receptor (TLR) signaling in macrophages and myeloid cells, which may be due to its ability to inhibit NF-κβ activation. Diethone is also involved in metabolic disorders such as bowel disease or liver disease. This compound is metabolized by rat liver microsomes and produces a number of

Fórmula: C₁₃H₁₉NO₄

Pureza: Min. 95%

Forma y color: Yellow Powder

Peso molecular: 253.29 g/mol

Ref: 3D-FD00103