15268
N-Boc-diethanolamine
≥98.0% (GC)
Synonym(s):
tert-Butyl N,N-bis(2-hydroxyethyl)carbamate
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About This Item
Empirical Formula (Hill Notation):
C9H19NO4
CAS Number:
Molecular Weight:
205.25
Beilstein:
4386562
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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.)
SMILES string
CC(C)(C)OC(=O)N(CCO)CCO
InChI
1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
InChI key
KMUNFRBJXIEULW-UHFFFAOYSA-N
Other Notes
Building block for the synthesis of cationic lipids, nucleosides, etc; monomer for synthesis of poly(urethanes)
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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J.M. Orban et al.
Journal of Polymer Science Part A: Polymer Chemistry, 37, 3441-3441 (1999)
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.
I. Solodin et al.
Synlett, 617-617 (1996)
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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