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About This Item
Empirical Formula (Hill Notation):
C9H19NO4
CAS Number:
Molecular Weight:
205.25
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4386562
InChI
1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
SMILES string
CC(C)(C)OC(=O)N(CCO)CCO
InChI key
KMUNFRBJXIEULW-UHFFFAOYSA-N
assay
≥98.0% (GC)
reaction suitability
reagent type: cross-linking reagent
refractive index
n20/D 1.460
density
1.085 g/mL at 20 °C (lit.)
Other Notes
Building block for the synthesis of cationic lipids, nucleosides, etc; monomer for synthesis of poly(urethanes)
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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J.M. Orban et al.
Journal of Polymer Science Part A: Polymer Chemistry, 37, 3441-3441 (1999)
I. Solodin et al.
Synlett, 617-617 (1996)
S C Bergmeier et al.
Nucleosides & nucleotides, 18(2), 227-238 (1999-03-06)
We have prepared a series of novel aza-acyclonucleosides as potential antiviral agents. These compounds were prepared from diethanolamine and the desired purine or pyrimidine base via a Mitsunobu coupling. No antiviral activity was observed against either HSV-1 or HCMV.
Cláudia D Raposo et al.
Polymers, 12(1) (2020-01-18)
Doxorubicin-loaded PLGA nanoparticles conjugated with a new galactose-based ligand for the specific recognition by human hepatoma cellular carcinoma cells (Hep G2) were successfully produced. The new targeting compound was selected using molecular docking combined with quantum chemical calculations for modelling
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