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Catalog Number:
12838
CAS Number:
137743-46-5
Boc-2-isothiocyanatoéthylamine
Purity:
≥ 95 % (RMN)
Synonym(s):
carbamate de tert- butyle n-(2-isothiocyanatoéthyle)
Documents
$67.60 /100 mg
Taille
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Product Information

Synthèse de 2-alkylamino-1-imidazolines.

Synonyms
carbamate de tert- butyle n-(2-isothiocyanatoéthyle)
CAS Number
137743-46-5
Purity
≥ 95 % (RMN)
Molecular Formula
C8H14N2O2S
Molecular Weight
202.28
MDL Number
MFCD00674499
PubChem ID
4219896
Melting Point
85-89 ?C
Appearance
Solide jaune pâle
Conditions
Conserver à 0-8 °C
General Information
Synonyms
carbamate de tert- butyle n-(2-isothiocyanatoéthyle)
CAS Number
137743-46-5
Purity
≥ 95 % (RMN)
Molecular Formula
C8H14N2O2S
Molecular Weight
202.28
MDL Number
MFCD00674499
PubChem ID
4219896
Melting Point
85-89 ?C
Appearance
Solide jaune pâle
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-2-isothiocyanatoethylamine is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of anticancer agents.
  • Bioconjugation: It is employed in the creation of bioconjugates, enhancing the specificity and efficacy of targeted therapies in cancer treatment.
  • Research in Neuroscience: The compound is used in studies related to neuroprotection, helping researchers understand mechanisms of neurodegenerative diseases.
  • Agricultural Chemistry: It finds application in developing agrochemicals, particularly as a potential pesticide, contributing to sustainable agriculture practices.
  • Analytical Chemistry: Boc-2-isothiocyanatoethylamine is utilized in analytical methods for detecting and quantifying specific biomolecules, aiding in various biochemical analyses.

Citations