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Merck
CN

15408

Sigma-Aldrich

N-叔丁氧羰基-1,3-丙二胺

≥97.0% (GC/NT)

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别名:
N-(3-氨基丙基)氨基甲酸叔丁酯, N-Boc-1,3-二氨基丙烷
线性分子式:
(CH3)3COCONH(CH2)3NH2
CAS号:
分子量:
174.24
Beilstein:
3588328
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥97.0% (GC/NT)

反应适用性

reagent type: cross-linking reagent

折射率

n20/D 1.454 (lit.)
n20/D 1.459

bp

203 °C (lit.)

mp

22 °C (lit.)

密度

0.998 g/mL at 20 °C (lit.)

官能团

Boc
amine

SMILES字符串

NCCCNC(OC(C)(C)C)=O

InChI

1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)

InChI key

POHWAQLZBIMPRN-UHFFFAOYSA-N

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应用

  • Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–carbohydrate conjugates′: This study discusses the synthesis of derivatives using N-Boc-1,3-propanediamine to develop new antibacterial agents targeting resistant bacterial strains (Yarlagadda et al., 2015).
  • Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022).
  • Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018).

其他说明

合成亚精胺类似物;制备药理活性化合物。

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Skin Corr. 1B

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

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


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T L Huang et al.
Journal of medicinal chemistry, 35(13), 2414-2418 (1992-06-26)
A number of substrate analogues of N8-acetylspermidine (N8-AcSpd) (16) and chemical modifying agents containing metal coordinating ligands were assayed as inhibitors of the cytoplasmic enzyme N8-AcSpd deacetylase from rat liver. The enzyme is inhibited by metal chelators, several omega-amino-substituted carboxylic
Hironori Abe et al.
The Journal of reproduction and development, 61(4), 277-286 (2015-05-01)
We recently demonstrated that luteal cells flow out from the ovary via lymphatic vessels during luteolysis. However, the regulatory mechanisms of the outflow of luteal cells are not known. Matrix metalloproteinases (MMPs) can degrade the extracellular matrix and basal membrane
B. Plouvier et al.
Heterocycles, 32, 693-693 (1991)
Syota Kawaguchi et al.
The Journal of reproduction and development, 59(3), 225-230 (2013-01-30)
Luteinizing hormone (LH) regulates several ovarian functions. However, the luteoprotective mechanisms of LH involved in the maintenance of bovine corpus luteum (CL) function are not well understood. Since prostaglandin F2α (PGF), PGE2 and progesterone (P4) are well documented as antiapoptotic
Syota Kawaguchi et al.
The Journal of reproduction and development, 59(3), 219-224 (2013-02-07)
Luteoprotective mechanisms of luteinizing hormone (LH) involved in the maintenance of bovine corpus luteum (CL) function have not been completely clarified. Since antioxidant enzymes are well documented as antiapoptotic factors in the CL of many mammals, we hypothesized that the

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