120227
Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
95%
Synonym(s):
Hantzsch ester
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About This Item
Empirical Formula (Hill Notation):
C13H19NO4
CAS Number:
Molecular Weight:
253.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-561-6
MDL number:
Assay:
95%
Form:
solid
Quality Level
assay
95%
form
solid
mp
178-183 °C (lit.)
solubility
organic solvents: soluble
functional group
ester
SMILES string
CCOC(=O)C1=C(C)NC(C)=C(C1)C(=O)OCC
InChI
1S/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
InChI key
LJXTYJXBORAIHX-UHFFFAOYSA-N
General description
Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate is often used as a building block in organic synthesis for the preparation of various biologically active compounds.
Application
Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate (DTP) was used to study the mechanism of electrochemical oxidation of DTP in ethanol/water solutions on a glassy carbon electrode.
Used as a hydrogen source in organocatalytic reductive amination and conjugate reduction.
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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V F Dubrovskaja et al.
Radiobiologia, radiotherapia, 31(1), 79-84 (1990-01-01)
Female mice (CBA X C57 Bl) F1 were exposed a single total-body gamma-irradiation with a dose efficiency of 6.5 Gy/min with doses of 2.5-7.5 Gy in air or inhaling a gas mixture of 6-6.5% oxygen and 94-93% nitrogen. All naturally
R Nosal et al.
Bratislavske lekarske listy, 102(10), 447-453 (2002-01-23)
Metabolites of arachidonic acid are important regulatory substances in blood platelets. They participate in platelet adhesion and aggregation, and pharmacological intervention with arachidonate cascade is widely used in therapy of hyperactive platelets and in the prevention of thromboembolic complications. To
Jing Zhang et al.
iScience, 23(1), 100755-100755 (2019-12-31)
The alkoxyl radical is an essential reactive intermediate in mechanistic studies and organic synthesis with hydrogen atom transfer (HAT) reactivity. However, compared with intramolecular 1,5-HAT or intermolecular HAT of alkoxyl radicals, the intramolecular 1,2-HAT reactivity has been limited to theoretical
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 120227-50G | 04061832540887 |
| 120227-10G | 04061838713551 |
| 120227-1G | 04061838713568 |