D94208
乙氧基亚甲基丙二酸二乙酯
99%
别名:
乙氧基甲基烯丙基酸二乙酯, 异烟肼
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关于此项目
线性分子式:
C2H5OCH=C(COOC2H5)2
化学文摘社编号:
分子量:
216.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-725-7
Beilstein/REAXYS Number:
880058
MDL number:
Assay:
99%
Form:
liquid
InChI key
LTMHNWPUDSTBKD-UHFFFAOYSA-N
InChI
1S/C10H16O5/c1-4-13-7-8(9(11)14-5-2)10(12)15-6-3/h7H,4-6H2,1-3H3
SMILES string
CCO\C=C(\C(=O)OCC)C(=O)OCC
assay
99%
form
liquid
refractive index
n20/D 1.462 (lit.)
bp
279-281 °C (lit.)
density
1.07 g/mL at 25 °C (lit.)
Quality Level
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Application
二乙基乙氧基甲基烯丙基酯可用作合成嘧啶酮、噻唑并嘧啶、噻唑并嘧啶酮、三唑并 [1,5-a] 嘧啶、嘧啶并 [2,1-b] 苯并噻唑和 3-氨基-5-氧代异恶唑烷-4-羧酸乙酯衍生物的前体。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1A
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
291.2 °F - closed cup
flash_point_c
144 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
An Efficient Cascade Synthesis of Ethyl 3-Amino-5-oxoisoxazolidine-4-carboxylate Derivatives.
Li R, et al.
Synthesis, 49(18), 4341-4349 (2017)
Synthesis and structure activity relationship investigation of triazolo [1, 5-a] pyrimidines as CB2 cannabinoid receptor inverse agonists.
Tabrizi M A, et al.
European Journal of Medicinal Chemistry, 113, 11-27 (2016)
Microwave Assisted Synthesis of Fused Thiazoles in Multicomponent System and Their in vitro Antitumor, Antioxidant, and Antimicrobial Activities.
El?Borai M A, et al.
Journal of Heterocyclic Chemistry, 54(2), 1031-1041 (2017)
Synthesis and in vitro antitumor activity of new series of benzothiazole and pyrimido [2, 1-b] benzothiazole derivatives.
Gabr M T, et al.
European Journal of Medicinal Chemistry, 85, 576-592 (2014)
Sergio Gómez-Alonso et al.
Journal of agricultural and food chemistry, 55(3), 608-613 (2007-02-01)
A method has been developed for the simultaneous analysis of biogenic amines, amino acids, and the ammonium ion in wine and beer. Aminoenones formed by the reaction of amino acids, biogenic amines, and the ammonium ion with the derivatization reagent
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