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Merck
CN

15369

Sigma-Aldrich

N-Boc-乙二胺

≥98.0% (NT)

别名:

N-(2-氨乙基)氨基甲酸叔丁酯, N-Boc-1,2-二氨基乙烷

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About This Item

线性分子式:
(CH3)3COCONHCH2CH2NH2
CAS号:
分子量:
160.21
Beilstein:
1932330
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥98.0% (NT)

反应适用性

reagent type: cross-linking reagent

折射率

n20/D 1.458 (lit.)
n20/D 1.458

沸点

72-80 °C/0.1 mmHg (lit.)

密度

1.012 g/mL at 20 °C (lit.)

官能团

Boc
amine

SMILES字符串

NCCNC(OC(C)(C)C)=O

InChI

1S/C7H16N2O2/c1-7(2,3)11-6(10)9-5-4-8/h4-5,8H2,1-3H3,(H,9,10)

InChI key

AOCSUUGBCMTKJH-UHFFFAOYSA-N

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应用

  • Facile synthesis of new N-(aminocycloalkylene) amino acid compounds:描述N-Boc-乙二胺在2-{[2-(Boc-氨基)乙基]氨基}乙酸苄酯制备中的应用(G Matulevičiūtė et al., 2023)。
  • Synthesis of a new tripod BODIPY dye:报道N-Boc-乙二胺参与化学合成BODIPY染料(H Wang et al., 2022)。
  • Single‐Entity Electrocatalysis:讨论N-Boc-乙二胺在电催化用改性Co3O4纳米颗粒中的应用(T Quast et al., 2021)。

其他说明

乙二胺的单保护衍生物,制备药理活性类似物;引入乙二胺间隔基。

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Russell D Viirre et al.
The Journal of organic chemistry, 68(4), 1630-1632 (2003-02-15)
An improved synthesis of ethyl N-[(2-Boc-amino)ethyl]glycinate and its hydrochloride salt is reported. The synthesis is based on the reductive alkylation of Boc-ethylenediamine with ethyl glyoxylate hydrate and furnishes the title compound in near quantitative yield and high purity without chromatography.
Deborah Sultan et al.
Small (Weinheim an der Bergstrasse, Germany), 14(30), e1703115-e1703115 (2018-07-03)
Focused ultrasound (FUS) technology is reported to enhance the delivery of 64 Cu-integrated ultrasmall gold nanoclusters (64 Cu-AuNCs) across the blood-brain barrier (BBB) as measured by positron emission tomography (PET). To better define the optimal physical properties for brain delivery
W S Saari et al.
Journal of medicinal chemistry, 34(10), 3132-3138 (1991-10-01)
Basic nitrobenzenesulfonamides containing nitroisopropyl and (ureidooxy)methyl groups were prepared and evaluated as novel hypoxic cell selective cytotoxic agents. In vitro, N-(2-aminoethyl)-N-methyl-3-nitro-4-(1-methyl-1-nitroethyl)benzene sulfonamide hydrochloride (11) proved to be preferentially toxic to hypoxic EMT6 mammary carcinoma cells. At 1 mM concentration in
E Morier-Teissier et al.
Journal of medicinal chemistry, 36(15), 2084-2090 (1993-07-23)
A new molecule 4 [(GGH-DAE)2DHQ] associating the 1,4,5,8-tetrahydroxyanthraquinone ring (DHQ) of the antitumor drug mitoxantrone (2), two diaminoethylene chains (DAE), and the metal-chelating peptide Gly-Gly-His (GGH) has been synthesized. Such a molecule presents characteristics able to induce antitumor activity: compound
Synthesis of N,N-dilactitol ethylenediamine: a versatile spacer for attachment of residualizing labels to protein.
M M Dowd et al.
Analytical biochemistry, 205(2), 369-371 (1992-09-01)

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