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Merck

W237507

Sigma-Aldrich

丙二酸二乙酯

≥98%, FG

别名:

胡萝卜酸二乙酯

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About This Item

线性分子式:
CH2(COOC2H5)2
CAS号:
分子量:
160.17
FEMA號碼:
2375
Beilstein:
774687
EC號碼:
歐洲委員會號碼:
2106
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
9.490
NACRES:
NA.21

生物源

synthetic

品質等級

等級

FG
Halal

agency

meets purity specifications of JECFA

法律遵循

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

蒸汽密度

5.52 (vs air)

蒸汽壓力

1 mmHg ( 40 °C)

化驗

≥98%

折射率

n20/D 1.413 (lit.)

bp

199 °C (lit.)

mp

−51-−50 °C (lit.)

密度

1.055 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

感官的

apple; green; fruity; sweet

SMILES 字串

CCOC(=O)CC(=O)OCC

InChI

1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3

InChI 密鑰

IYXGSMUGOJNHAZ-UHFFFAOYSA-N

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一般說明

丙二酸二乙酯是一种活性亚甲基化合物,可在食品工业中用作调味剂。

應用


  • Synthesis and biological activities of novel structural analogues of 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand.: This study by Suhara et al. focuses on the synthesis of novel structural analogues of 2-arachidonoylglycerol, an endogenous ligand for cannabinoid receptors. The research highlights the utilization of diethyl malonate in the synthesis process, emphasizing its importance in creating biologically active compounds with potential therapeutic applications in modulating cannabinoid receptor activity (Suhara et al., 2001).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

199.4 °F - closed cup

閃點(°C)

93 °C - closed cup

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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其他客户在看

Slide 1 of 1

1 of 1

Encyclopedia of Food and Color Additives, 1, 818-818 (1997)
Encyclopedia of Food and Color Additives, 1, 818-818 (1997)
Shigeyuki Yamada et al.
Organic & biomolecular chemistry, 5(9), 1442-1449 (2007-04-28)
The addition of heteroaromatic lithium reagents 2 to a THF solution of perfluorocyclopentene (1) provided preferentially the corresponding monosubstituted products 5, while the addition of 1 to 2 effectively gave the 1,2-disubstituted products 6 in good to excellent yields. The
Sau Fan Yip et al.
Organic letters, 9(17), 3469-3472 (2007-07-20)
An effective method in targeting alpha-aryl malonates is reported. In the presence of a catalytic amount of 2-picolinic acid and CuI, the coupling of aryl iodides with diethyl malonate proceeds smoothly even at room temperature. The high levels of functional
Lian Jin Liu et al.
Nucleosides, nucleotides & nucleic acids, 30(10), 784-797 (2011-10-05)
Novel 5'-norcarbocyclic adenosine phosphonic acid analogues with 6'-electropositive moiety such as spirocyclopropane were designed and synthesized from the commercially available diethylmalonate 5. Regioselective Mitsunobu reaction proceeded in the presence of an allylic functional group at a low reaction temperature in

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