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120227

Sigma-Aldrich

二乙基-1,4-二氢-2,6-二甲基-3,5-吡啶二羧酸酯

95%

同義詞:

二氢吡啶

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About This Item

經驗公式（希爾表示法）:
C13H19NO4
CAS號碼:
1149-23-1
分子量：:
253.29
EC號碼:
214-561-6
MDL號碼:
MFCD00005951
分類程式碼代碼:
12352100
PubChem物質ID:
24847411
NACRES:
NA.22

品質等級

100

化驗

95%

形狀

solid

mp

178-183 °C (lit.)

溶解度

organic solvents: soluble

官能基

ester

SMILES 字串

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 密鑰

LJXTYJXBORAIHX-UHFFFAOYSA-N

相關類別

一般說明

二乙基1,4-二氢-2,6-二甲基-3,5-吡啶二羧酸酯常被用作有机合成中的合成砌块，用于制备各种生物活性化合物。

應用

二乙基-1,4-二氢-2,6-二甲基-3,5-吡啶二羧酸酯（DTP）被用于研究乙醇/水溶液中的DTP在玻璃碳电极上的电化氧化机理。
用作有机催化还原胺化反应和共轭还原反应的氢源。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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分析證明 (COA)

Lot/Batch Number
MKCM2363
MKCG9624
MKBZ9906V
MKBW1988V
MKBS5567V

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[Geroprotective activity of 2,6-dimethyl-3,5-diethoxycarbonyl-l,4-dihydropyridine].
N M Emanuél' et al.
Doklady Akademii nauk SSSR, 284(5), 1271-1274 (1985-01-01)
M V Bilenko et al.
Biulleten' eksperimental'noi biologii i meditsiny, 96(9), 8-11 (1983-09-01)
Prophylactic injection of the natural antioxidant alpha-tocopherol and synthetic antioxidants ionol, diludin and 6-mercurascan prevented the development of lesions during acute renal ischemia and subsequent reperfusion. Ionol proved more effective on intraperitoneal injection than on intragastric route of administration. It
M Mamadiev et al.
Voprosy meditsinskoi khimii, 29(2), 83-89 (1983-03-01)
Appearance of cadaverine deaminating activity in mitochondrial fractions of liver and kidney of rabbits with experimental alimentary hypercholesterolaemia was prevented by an antioxant diludin (2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine) which also decreased the abnormally elevated AMP-deaminating activity and elevated the decreased monoamine oxidase activity
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
N A Basova et al.
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova, 88(5), 650-657 (2002-07-26)
The main concern of this work was to examine the relation between altered antioxidant status on the one hand and increase in L-tryptophan absorption in the small intestine in order to bring further information regarding to possible role of vitamin
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