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

Product Details

CAS No:1149-23-1

MF:C13H19NO4

Appearance:light-yellow or yellow crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:MT

Synonyms:DIETHYL 2,6-DIMETHYL-1,4-DIHYDROPYRIDINEDICARBOXYLATE;DIETHYL 1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLATE;AURORA 4780;3,5-DICARBETHOXY-2,6-DIMETHYL-1,4-DIHYDROPYRIDINE;3,5-BIS(CARBOETHOXY)-2,6-DIMETHYL-1,4-DIHYDROPYRIDINE;1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID DIETHYL ESTER;RARECHEM AQ NN 0171;5-pyridinedicarboxylicacid,1,4-dihydro-2,6-dimethyl-diethylester; 1149-23-1; Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate; Etidin; Hantzsch ester; Diethone; Hantzsch's dihydropyridine; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-, diethyl ester; diludin; GWN6123BUG; 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine; DTXSID80150895; 2,6-dimethyl-3,5-dicarbethoxy-1,4-dihydropyridine; ethidin; DM-DEOC-DHP; RefChem:139231; DTXCID4073386; Diludine; Ethidine; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; MFCD00005951; NSC 3344; RR 116; NSC 120573; Diethyl 2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate; 3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine; 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Diethyl Ester; 3,5-diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; MLS000737519; Diethyl 1,4-dihydro-2,6-dimethyl-3-5-pyridinedicarboxylate; Diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate; 2,6-Dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester; NSC-3344; 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine; NSC-120573; 3,5-Bis(ethoxycarbonyl)-1,4-dihydro-2,6-dimethylpyridine; 3,5-Diethoxycarbonyl-1,4-dihydro-2,6-dimethylpyridine; ethyl 5-(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate; 3, 1,4-dihydro-2,6-dimethyl-, diethyl ester; SR-01000314518; EINECS 214-561-6; UNII-GWN6123BUG; AI3-61863; RR-116; Maybridge1_005647; ChemDiv2_005231; Oprea1_780789; SCHEMBL95164; MLS000060889; DivK1c_001935; orb3025652; SCHEMBL9548052; SCHEMBL9548059; CHEMBL1521734; CHEMBL3194512; HMS557I15; Diethyl1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate; MSK8058; NSC3344; HMS1383N17; HMS2399L03; HMS2884B15; ALBB-018041; EBC-46084; NSC120573; s5221; SBB001546; STK723901; 2,6-DIMETHYL-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLIC ACID DIETHYL ESTER; AKOS000593008; AB00545; AC-5634; CCG-207953; CS-W018746; FD00103; GS-3120; CDS1_000895; IDI1_003946; SMR000069117; SMR000528546; ST075583; SY016910; DB-005424; D3775; NS00023724; ST50230605; EN300-26986; VU0007198-5; AG-205/25020007; F076860; DIETHYL 1,4-DIHYDRO-3,5-PYRIDINECARBOXYLATE; SR-01000314518-1; SR-01000314518-2; 1,4-dihydro-3,5-dicarbethoxy-2,6-dimethyl pyridine; Q27279321; Z57393194; Diethyl 26-dimethyl-14-dihydropyridine-35-dicarboxylate; F0191-0461; 1,4-DIHYDRO-3,5-DICARBETHOXY-2,6-DIMETHYLPYRIDINE; 2,6-Dimethyl-3,5-bis(ethoxycarbonyl)-1,4-dihydropyridine; 3,5-bis(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine; diethyl 1,4-dihydro-2,6-dimethy-3,5 pyridinedicarboxylate; diethyl 2,6-dimethyl-l,4-dihydro-3,5-pyridinedicarboxylate; Diethyl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate; diethyl-1,4-dihydro-2,6-dimethyl-3.5-pyridinedicarboxylate; 2,6-DIMETHYL-3,5-DI(CARBOETHOXY)-1,4-DIHYDROPYRIDINE; 3,5-DIETHOXYCARBONYL-2,6-DIMETHYL-1,4-DIHYDROPYRIDINE; diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridine dicarboxylate; diethyl 2,6-dimethyl-1,4-dihydro-3,5-pyridine dicarboxylate; Diethyl 2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate #; diethyl-1,4-dihydro-2,6-dimethyl-3,5-pyridine dicarboxylate; diethyl-1,4-dihydro-2,6-dimethyl-3.5-pyridine dicarboxylate; Ethyl (2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate); Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate, 95%; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-,diethyl ester; 1,4-DIHYDRO-3,5-DICARBOXYLIC ACID DIETHYL ESTER-2,6-DIMETHYLPYRIDINE; 3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-, 3,5-DIETHYL ESTER; 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine ; 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester; 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine; 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester

Product application:Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate,1149-23-1,Diludine,Hantzsch ester,Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate,1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester,Ethidine,Etidin,Pharmaceutical grade Hantzsch ester,Organocatalytic hydrogen source,Biomimetic NADH surrogate,Asymmetric transfer hydrogenation reagent,Imine reduction reagent,Chiral amine synthesis synthon,Feed grade diludine,Antioxidant feed additive,Anti-heat stress additive,Photocatalytic reduction reagent,High purity Hantzsch ester 99.5%,Low pyridine impurity diludine,CAS 1149-23-1 supplier,Diludine manufacturer China,Suzhou Health Chemicals specialty chemicals,Hantzsch ester wholesale bulk export

 

Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate is widely utilized across biomimetic catalytic organic reductions, asymmetric pharmaceutical transfer hydrogenations, photoredox single-electron donor transformations, functional polymer stabilization, and commercial agricultural livestock and aquaculture antioxidant feed supplementation sectors. In synthetic organic chemistry and medicinal process development, universally recognized across chemical research as Hantzsch ester or Diludine, it serves as a quintessential synthetic surrogate for the biochemical reducing coenzyme NADH; driven by the thermodynamic driving force of aromatization to a pyridine core, it donates hydride equivalents under mild, transition-metal-free conditions, coupling with chiral organocatalysts such as chiral phosphoric acids to accomplish highly enantioselective transfer hydrogenations of imines, electron-deficient alkenes, and heterocyclic systems to assemble chiral amines and bioactive pharmaceutical building blocks; in modern visible-light photoredox and radical cross-coupling methodology, it operates as an effective single-electron transfer agent and hydrogen atom transfer donor for functional group activations; in agronomic animal science and livestock nutrition, it is formulated into premixes as a multifunctional non-hormonal metabolic and antioxidant feed additive, inhibiting lipid peroxidation across cellular biomembranes, shielding endogenous vitamins A and E from oxidative degradation, and modulating the neuroendocrine axis to alleviate physiological heat stress in dairy livestock, poultry, and aquaculture stocks while optimizing nutrient assimilation and growth performance; furthermore, in specialty materials engineering, Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate functions as a thermal and oxidative stabilizer for functional elastomers and polyolefins to prevent oxidative embrittlement.