Name: <I>N</I>-叔丁氧羰基-1,3-丙二胺
Brand: ALDRICH

登录查看公司和协议定价

线性分子式:

(CH₃)₃COCONH(CH₂)₃NH₂

CAS Number:

分子量:

174.24

Beilstein:

3588328

MDL编号:

UNSPSC代码:

12352116

PubChem化学物质编号:

NACRES:

NA.22

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

≥97.0% (GC/NT)

reagent type: cross-linking reagent

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

203 °C (lit.)

22 °C (lit.)

0.998 g/mL at 20 °C (lit.)

Boc
amine

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

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

POHWAQLZBIMPRN-UHFFFAOYSA-N

正在寻找类似产品? 访问产品对比指南

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).