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Catalog Number:
20577
CAS Number:
179688-01-8
7-Benzyloxy-6-methoxy-3H-quinazolin-4-one
Purity:
≥ 98% (HPLC)
Synonym(s):
7-(Benzyloxy)-6-methoxy-4(3H-quinazolinone
Documents
$139.11 /100MG
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Product Information

7-Benzyloxy-6-methoxy-3H-quinazolin-4-one is a versatile compound recognized for its significant applications in medicinal chemistry and pharmaceutical research. This compound features a unique quinazolinone structure, which is known for its potential as a scaffold in drug development. Its ability to interact with various biological targets makes it a valuable candidate for the synthesis of novel therapeutic agents. Researchers have explored its efficacy in anti-cancer and anti-inflammatory applications, showcasing its potential to contribute to the development of effective treatments.

In addition to its medicinal properties, 7-Benzyloxy-6-methoxy-3H-quinazolin-4-one serves as an important intermediate in organic synthesis, facilitating the creation of complex molecules. Its favorable solubility and stability under various conditions enhance its utility in laboratory settings. This compound is particularly beneficial for researchers looking to innovate in drug discovery, as it offers a promising pathway to developing new pharmaceuticals with improved efficacy and safety profiles.

Synonyms
7-(Benzyloxy)-6-methoxy-4(3H-quinazolinone
CAS Number
179688-01-8
Purity
≥ 98% (HPLC)
Molecular Formula
C16H14N2O3
Molecular Weight
282.3
MDL Number
MFCD04115119
PubChem ID
135404718
Melting Point
> 245 °C
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
7-(Benzyloxy)-6-methoxy-4(3H-quinazolinone
CAS Number
179688-01-8
Purity
≥ 98% (HPLC)
Molecular Formula
C16H14N2O3
Molecular Weight
282.3
MDL Number
MFCD04115119
PubChem ID
135404718
Melting Point
> 245 °C
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

7-Benzyloxy-6-methoxy-3H-quinazolin-4-one is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents due to its ability to inhibit specific cellular pathways.
  • Biological Research: It is used in studies investigating the mechanisms of action of quinazoline derivatives, aiding researchers in understanding their biological activities and potential therapeutic effects.
  • Drug Formulation: The compound can be incorporated into drug formulations to enhance solubility and bioavailability, making it a valuable asset in the formulation of oral medications.
  • Material Science: Its unique chemical structure allows it to be explored in the development of novel materials, such as organic light-emitting diodes (OLEDs), which are used in advanced display technologies.
  • Analytical Chemistry: The compound is utilized as a reference standard in analytical methods, helping laboratories ensure the accuracy and reliability of their testing procedures for related compounds.

Citations