749648
2-[2-(Boc-amino)ethoxy]ethanol
97%
Synonym(s):
2-(2-tert-Butoxycarbonylaminoethoxy)ethanol, N-[2-(2-Hydroxyethoxy)ethyl]carbamic acid tert-butyl ester, tert-Butyl[2-(2-hydroxyethoxy)ethyl]carbamate, [2-(2-Hydroxyethoxy)ethyl]carbamic acid 1,1-dimethylethyl ester
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About This Item
Empirical Formula (Hill Notation):
C9H19NO4
CAS Number:
Molecular Weight:
205.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
liquid
Quality Segment
assay
97%
form
liquid
refractive index
n
density
1.061 g/mL at 25 °C
functional group
amine, ether, hydroxyl
SMILES string
CC(C)(C)OC(=O)NCCOCCO
InChI
1S/C9H19NO4/c1-9(2,3)14-8(12)10-4-6-13-7-5-11/h11H,4-7H2,1-3H3,(H,10,12)
InChI key
KSFVNEXYCULLEJ-UHFFFAOYSA-N
Application
2-[2-(Boc-amino)ethoxy]ethanol is N-terminal protected 2-(2-aminoethoxy)ethanol. It is generally used as a molecular spacer/linker. Some of such applications are:
- Synthesis of biotinylated HaloLigands to prepare quantum dot adducts for HaloTag protein-mediated specific labeling of live cells.
- It is one of the key precursors for the total synthesis of tyroscherin and photo-activatable tyroscherin-based affinity reagent used for identification of tyroscherin binding proteins.
- It can be used to link HaloTag enzyme with fluorescent zinc indicator, ZIMIR to monitor the dynamics of regulated secretion of zinc in real time.
- It can also be used to synthesize amphiphiles for DNA and siRNA delivery.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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