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Merck
CN

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
Beilstein:
5331567
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
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Assay

≥98.0% (GC)

reaction suitability

reagent type: cross-linking reagent

mp

92-96 °C

SMILES string

CC(C)(C)OC(=O)NCCN=C=S

InChI

1S/C8H14N2O2S/c1-8(2,3)12-7(11)10-5-4-9-6-13/h4-5H2,1-3H3,(H,10,11)

InChI key

FWYDKMQRTRGCPC-UHFFFAOYSA-N

Application

Used in the synthesis of 2-alkylamino-1-imidazolines

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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D.M. Perrault et al.
Tetrahedron, 51, 353-353 (1995)
K. Ariga et al.
The Journal of Organic Chemistry, 57, 417-417 (1992)
Gamze Dereli Can et al.
Cytotherapy, 21(1), 83-95 (2018-12-05)
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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