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 Segment
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