跳转至内容
Merck
CN

121967

Sigma-Aldrich

氨基乙醛缩二甲醇

99%

登录查看公司和协议定价

别名:
2,2-二甲氧基乙胺
线性分子式:
NH2CH2CH(OCH3)2
CAS号:
分子量:
105.14
Beilstein:
741868
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

折射率

n20/D 1.417 (lit.)

bp

135-139 °C/95 mmHg (lit.)

密度

0.965 g/mL at 25 °C (lit.)

SMILES字符串

COC(CN)OC

InChI

1S/C4H11NO2/c1-6-4(3-5)7-2/h4H,3,5H2,1-2H3

InChI key

QKWWDTYDYOFRJL-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

氨基乙醛缩二甲醇与砜反应,然后加入所需的哌嗪衍生物进行水解和还原胺化反应,从而产生2-呋喃基[1,2,4]三唑并[1,5-a][1,3,5]三嗪的哌嗪衍生物.

氨基乙醛二甲基缩醛可用作合成各种酰化和磺化氧代烯酰胺(oxyenamide)的合成砌块。

应用

氨基乙醛缩二甲醇被用于开发醛脱氢酶的荧光底物。它被用于制备具有羧基、酯和聚乙二醇等各种官能团的壳聚糖-树枝状大分子杂化物。它被用于从 L-抗坏血酸 合成双环脯氨酸类似物的高效3步合成法,并用于MgClO4 催化的三组分反应,得到α-氨基膦酸盐

象形图

FlameCorrosion

警示用语:

Danger

危险声明

危险分类

Flam. Liq. 3 - Skin Corr. 1B

WGK

WGK 2

闪点(°F)

111.2 °F

闪点(°C)

44 °C

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Stereoselective Synthesis of 2-Oxyenamides
Krieg, Sara-Cathrin and Grimmer
European Journal of Organic Chemistry (2022)
Chi B Vu et al.
Bioorganic & medicinal chemistry letters, 14(19), 4835-4838 (2004-09-03)
Piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine have recently been shown to be potent and selective adenosine A(2a) receptor antagonists. We now demonstrate that potent and selective A(2a) receptor antagonists could still be obtained when the arylpiperazines are separated from the triazolotriazine core
Improved synthesis of imidazole-2-carboxaldehyde, imidazole-2-carboxylic acid, and ethyl imidazole-2-carboxylate
Galeazzi, Eduviges and Guzman
The Journal of Organic Chemistry, 60, 1090-1092 (1995)
Hitoshi Sashiwa et al.
Biomacromolecules, 4(5), 1244-1249 (2003-09-10)
Chitosan-dendrimer hybrids having various functional groups such as carboxyl, ester, and poly(ethylene glycol) groups were prepared successfully using dendrimer acetal by reductive N-alkylation. The synthetic procedure could be accomplished by one-step reaction without organic solvent. The degree of substitution of
R W Storms et al.
Proceedings of the National Academy of Sciences of the United States of America, 96(16), 9118-9123 (1999-08-04)
Because hematopoietic stem cells are rich in aldehyde dehydrogenase (ALDH) activity, we developed a fluorescent substrate for ALDH, termed BODIPY aminoacetaldehyde (BAAA), and tested its potential for isolating primitive human hematopoietic cells. A population of cells with low orthogonal light

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门