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Catalog Number:
16905
CAS Number:
145013-05-4
N , N -Di-( tert -Butoxycarbonyl)thiourée
Purity:
≥ 98 % (HPLC)
Synonym(s):
Bis-Boc-thiourée
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Product Information

N,N'-Di-(tert-Butoxycarbonyl)thiourea is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This thiourea derivative is particularly valued for its ability to act as a protecting group for amines and thiols, facilitating the selective functionalization of complex molecules. Its robust stability under various reaction conditions makes it an ideal choice for researchers looking to streamline synthetic pathways in the development of biologically active compounds.

In addition to its role in protecting group chemistry, N,N'-Di-(tert-Butoxycarbonyl)thiourea has shown potential in the synthesis of peptide derivatives and other nitrogen-containing heterocycles, which are crucial in drug discovery and development. Its unique structure allows for enhanced solubility and reactivity, making it a preferred reagent in various organic transformations. Researchers and industry professionals can leverage this compound to improve yields and simplify purification processes, ultimately accelerating the pace of innovation in their projects.

Synonyms
Bis-Boc-thiourée
CAS Number
145013-05-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H20N2O4S
Molecular Weight
276.4
MDL Number
MFCD03093917
PubChem ID
5193990
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
Bis-Boc-thiourée
CAS Number
145013-05-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H20N2O4S
Molecular Weight
276.4
MDL Number
MFCD03093917
PubChem ID
5193990
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N,N'-Di-(tert-Butoxycarbonyl)thiourea is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Protecting Groups in Chemistry: It acts as a protecting group for amines and thiols during chemical reactions, allowing for selective transformations without unwanted side reactions.
  • Peptide Synthesis: In the field of biochemistry, it is employed in peptide synthesis, enhancing the stability and solubility of intermediates, which is crucial for successful reactions.
  • Research in Material Science: The compound is explored for its potential applications in creating advanced materials, particularly in the development of polymers with specific properties.
  • Drug Development: Its role in drug formulation helps improve the bioavailability of active pharmaceutical ingredients, making it a valuable asset in the pharmaceutical industry.

Citations