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Catalog Number:
37786
CAS Number:
2892-62-8
3,4-Dibutoxi-3-ciclobuteno-1,2-diona
Purity:
≥ 98% (GC)
Synonym(s):
Escuarato de dibutilo, Triste
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Product Information

Conservar bajo gas inerte.

Synonyms
Escuarato de dibutilo, Triste
CAS Number
2892-62-8
Purity
≥ 98% (GC)
Molecular Formula
C12H18O4
Molecular Weight
226.27
MDL Number
MFCD00037150
PubChem ID
65108
Density
1.05 (Literatura)
Appearance
Líquido de color amarillo a marrón.
Boiling Point
139 °C / 0,5 mmHg (Literatura)
Refractive Index
n20/D 1.49 (Literatura)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Escuarato de dibutilo, Triste
CAS Number
2892-62-8
Purity
≥ 98% (GC)
Molecular Formula
C12H18O4
Molecular Weight
226.27
MDL Number
MFCD00037150
PubChem ID
65108
Density
1.05 (Literatura)
Appearance
Líquido de color amarillo a marrón.
Boiling Point
139 °C / 0,5 mmHg (Literatura)
Refractive Index
n20/D 1.49 (Literatura)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,4-Dibutoxy-3-cyclobutene-1,2-dione is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile intermediate in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Material Science: It is used in the development of advanced materials, particularly in coatings and polymers, where its unique properties enhance durability and performance.
  • Pharmaceutical Development: The compound plays a role in drug formulation, where its chemical properties can improve the solubility and bioavailability of active pharmaceutical ingredients.
  • Photochemical Applications: It is applied in photochemical reactions, benefiting industries that require light-sensitive materials, such as in the production of photoresists for electronics.
  • Research in Catalysis: This chemical is explored as a potential catalyst in various reactions, offering advantages like increased reaction rates and selectivity compared to traditional catalysts.

Citas