15524
N-Boc-2-isothiocyanatoethylamine
≥98.0% (GC)
Synonym(s):
tert-Butyl N-(2-isothiocyanatoethyl)carbamate
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About This Item
Empirical Formula (Hill Notation):
C8H14N2O2S
CAS Number:
Molecular Weight:
202.27
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5331567
InChI
1S/C8H14N2O2S/c1-8(2,3)12-7(11)10-5-4-9-6-13/h4-5H2,1-3H3,(H,10,11)
SMILES string
CC(C)(C)OC(=O)NCCN=C=S
InChI key
FWYDKMQRTRGCPC-UHFFFAOYSA-N
assay
≥98.0% (GC)
reaction suitability
reagent type: cross-linking reagent
mp
92-96 °C
Application
Used in the synthesis of 2-alkylamino-1-imidazolines
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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K. Ariga et al.
The Journal of Organic Chemistry, 57, 417-417 (1992)
D.M. Perrault et al.
Tetrahedron, 51, 353-353 (1995)
Gamze Dereli Can et al.
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Several methods to cultivate limbal epithelial stem cells (LESCs) in vitro with the support of feeder layers and different growth medium formulations have been established for several years. The initial green medium consists of various ingredients that exhibit a non-optimal
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