所有图片(1)
About This Item
线性分子式:
CH2(COOC2H5)2
CAS号:
分子量:
160.17
FEMA编号:
2375
Beilstein:
774687
EC 号:
欧洲委员会编号:
2106
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
9.490
NACRES:
NA.21
性状检查:
apple; green; fruity; sweet
等级:
FG
Halal
Halal
生物来源:
synthetic
Agency:
meets purity specifications of JECFA
食品过敏原:
no known allergens
推荐产品
生物来源
synthetic
质量水平
等级
FG
Halal
Agency
meets purity specifications of JECFA
管理合规性
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515
蒸汽密度
5.52 (vs air)
蒸汽压
1 mmHg ( 40 °C)
方案
≥98%
折射率
n20/D 1.413 (lit.)
沸点
199 °C (lit.)
mp
−51-−50 °C (lit.)
密度
1.055 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
apple; green; fruity; sweet
SMILES字符串
CCOC(=O)CC(=O)OCC
InChI
1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3
InChI key
IYXGSMUGOJNHAZ-UHFFFAOYSA-N
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一般描述
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。
应用
- 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).
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
199.4 °F - closed cup
闪点(°C)
93 °C - closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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
Hua Li et al.
Nucleosides, nucleotides & nucleic acids, 29(8), 581-590 (2010-07-28)
This article describes a very simple route for synthesizing novel lipophilic phosphonate bis(t-bu-SATE) prodrugs of acyclic cyclopentenylated nucleosides such as adenine 17 and cytosine 18. The key intermediate 6 was constructed via a ring-closing metathesis of compound 5, which could
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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