15408
N-叔丁氧羰基-1,3-丙二胺
≥97.0% (GC/NT)
别名:
N-(3-氨基丙基)氨基甲酸叔丁酯, N-Boc-1,3-二氨基丙烷
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关于此项目
线性分子式:
(CH3)3COCONH(CH2)3NH2
化学文摘社编号:
分子量:
174.24
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3588328
Assay:
≥97.0% (GC/NT)
Quality Level
assay
≥97.0% (GC/NT)
reaction suitability
reagent type: cross-linking reagent
refractive index
n20/D 1.454 (lit.), n20/D 1.459
bp
203 °C (lit.)
mp
22 °C (lit.)
density
0.998 g/mL at 20 °C (lit.)
functional group
Boc, amine
SMILES string
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
Application
- 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).
Other Notes
合成亚精胺类似物；制备药理活性化合物。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Inhibition of N8-acetylspermidine deacetylase by active-site-directed metal coordinating inhibitors.
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
B. Plouvier et al.
Heterocycles, 32, 693-693 (1991)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 15408-1ML | 04061838118103 |
| 15408-5ML | 04061838118110 |