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Catalog Number:
12958
CAS Number:
42855-00-5
Chloroformiate de 6-nitrovératryle
Purity:
≥ 97%
Synonym(s):
Chloroformiate de 4,5-diméthoxy-2-nitrobenzyle, Chlorure de 6-nitro-vératryloxycarbonyle
Hazmat
Documents
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Product Information

Réactif pour introduire le groupe amino-protecteur photo-clivable

Synonyms
Chloroformiate de 4,5-diméthoxy-2-nitrobenzyle, Chlorure de 6-nitro-vératryloxycarbonyle
CAS Number
42855-00-5
Purity
≥ 97%
Molecular Formula
C10H10ClNO6
Molecular Weight
275.64
MDL Number
MFCD00143507
PubChem ID
3084878
Melting Point
125 - 133 ?C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Chloroformiate de 4,5-diméthoxy-2-nitrobenzyle, Chlorure de 6-nitro-vératryloxycarbonyle
CAS Number
42855-00-5
Purity
≥ 97%
Molecular Formula
C10H10ClNO6
Molecular Weight
275.64
MDL Number
MFCD00143507
PubChem ID
3084878
Melting Point
125 - 133 ?C
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Nitroveratryl chloroformate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Bioconjugation: It is used for attaching biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Fluorescent Probes: The compound can be employed in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Polymer Chemistry: It acts as a coupling agent in the formulation of polymer materials, improving their properties for applications in coatings, adhesives, and composites.
  • Drug Development: Its unique reactivity makes it valuable in the modification of drug candidates, potentially improving their efficacy and bioavailability in therapeutic applications.

Citations