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氨基丙二酸二乙酯盐酸盐

氨基丙二酸二乙酯盐酸盐用途

【用途一】
用作医药中间体，用于合成嘧啶类杂环化合物

氨基丙二酸二乙酯盐酸盐名称

[ CAS 号 ]:
13433-00-6

[ 中文名 ]:
氨基丙二酸二乙酯盐酸盐

[ 英文名 ]:
Aminomalonamid

[中文别名 ]:

[英文别名 ]:

Diethyl aminomalonate hydrochloride
EINECS 236-556-8
Aminomalonic Acid Diethyl Ester Hydrochloride
Diethyl aminomalonate hydrochloride (1:1)
diethyl aminopropanedioate hydrochloride (1:1)
Diethyl 2-aminomalonate hydrochloride
MFCD00012510
Aminomalonamid

氨基丙二酸二乙酯盐酸盐物理化学性质

[ 密度 ]:
1.129 g/cm3

[ 沸点 ]:
156 - 158ºC

[ 熔点 ]:
165-170 °C (dec.)(lit.)

[ 分子式 ]:
C₇H₁₄ClNO₄

[ 分子量 ]:
211.643

[ 闪点 ]:
52.3ºC

[ 精确质量 ]:
211.061142

[ PSA ]:
78.62000

[ LogP ]:
0.94220

[ 外观性状 ]:
白色结晶针状

[ 蒸汽压 ]:
0.332mmHg at 25°C

[ 储存条件 ]:
2~8℃

[ 水溶解性 ]:
soluble

氨基丙二酸二乙酯盐酸盐MSDS

氨基丙二酸二乙酯盐酸盐安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2922499990

氨基丙二酸二乙酯盐酸盐合成路线

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氨基丙二酸二乙酯盐酸盐上游产品

氨基丙二酸二乙酯盐酸盐下游产品

氨基丙二酸二乙酯盐酸盐海关

[ 海关编码 ]: 2922499990

[ 中文概述 ]:
2922499990 其他氨基酸及其酯及它们的盐（含有一种以上含氧基的除外）. 增值税率:17.0% 退税率:9.0% 监管条件:AB(入境货物通关单,出境货物通关单) 最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

[ 监管条件 ]: A.入境货物通关单 B.出境货物通关单

[ 检验检疫 ]: P.进境动植物、动植物产品检疫 Q.出境动植物、动植物产品检疫 R.进口食品卫生监督检验 S.出口食品卫生监督检验 M.进口商品检验 N.出口商品检验

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

氨基丙二酸二乙酯盐酸盐文献

A heterocycle-forming double michael reaction. [5 + 1] annulation route to highly substituted and functionalized piperidines.

Org. Lett. 3(18) , 2911-4, (2001)

[reaction: see text]. Nitrogen-containing tethered diacids, easily prepared by reductive alkylation of diethyl aminomalonate or ethyl cyanoglycinate, undergo double Michael reactions with 3-butyn-2-on...

Reaction control in the organocatalytic asymmetric one-pot, three-component reaction of aldehydes, diethyl alpha-aminomalonate and nitroalkenes: toward diversity-oriented synthesis.

Chemistry 14(32) , 9873-7, (2008)

Spectroscopic studies of quinonoid species from pyridoxal 5'-phosphate.

Biochemistry 27(13) , 4923-33, (1988)

To establish the state of protonation of quinonoid species formed nonenzymically from pyridoxal phosphate (PLP) and diethyl aminomalonate, we have studied absorption spectra of the rapidly established...

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