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CAS 28957-72-4

N-Benzylnortropinone TCI B4058

N-Benzylnortropinone TCI B4058

Chemical Identity

CAS No.
28957-72-4
PubChem
CID 119846·SID 253659594
Formula
C14H17NO
Molecular weight
215.29 g/mol
Purity
>95.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
8-benzyl-8-azabicyclo[3.2.1]octan-3-one
SMILES
C1CC2CC(=O)CC1N2CC3=CC=CC=C3
InChIKey
RSUHKGOVXMXCND-UHFFFAOYSA-N
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N-Benzylnortropinone is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules. As a building block, it serves as a foundational material that can be modified through various chemical reactions to produce a wide range of compounds. This compound is especially valuable in the creation of heterocyclic structures and other complex molecules that require carbon modification. Its versatility makes it a key component in many synthetic pathways within chemical laboratories.

The compound's molecular structure is stable, allowing it to react with a variety of reagents such as acids, bases, and catalysts. This reactivity, combined with its predictable chemical behavior, makes it a preferred choice for researchers aiming to control and optimize chemical reactions. Its ability to participate in multiple reaction types enhances its utility in both academic and industrial settings.

In Indonesian laboratories, N-Benzylnortropinone is commonly used in organic chemistry research, particularly in pharmacology and the synthesis of bioactive compounds. Its availability and effectiveness in complex reactions make it a popular choice for researchers looking to accelerate the development of new compounds and improve experimental outcomes.

  • Organic synthesis is a key application where N-Benzylnortropinone is used to build complex molecular structures through various chemical reactions.
  • Pharmaceutical research benefits from this compound as it is involved in the synthesis of bioactive compounds and drug development processes.
  • Heterocyclic compound synthesis relies on N-Benzylnortropinone due to its ability to participate in carbon modification reactions.
  • Chemical modification studies often use this compound to explore new reaction pathways and functional group transformations.
  • Research in medicinal chemistry utilizes N-Benzylnortropinone to develop new therapeutic agents with specific biological activities.

Brand TCI
CAS number 28957-72-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

N-Benzylnortropinone should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep it in a tightly sealed container to prevent exposure to air and humidity. The compound is typically stored in glass or plastic containers that are resistant to chemical reactions. In a laboratory setting, it is important to handle the compound with appropriate personal protective equipment to ensure safety. Proper ventilation should be maintained when working with this compound to minimize inhalation risks. Always follow standard laboratory safety protocols when handling and storing chemical substances.

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