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Catalog Number:
41608
CAS Number:
171623-07-7
( R )- N -Boc-1-oxa-4-azaspiro[4.5]décane-3-carboxaldéhyde
Purity:
≥ 94% (CG)
Synonym(s):
Ester 1,1-diméthyléthylique de l'acide (3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylique, ( R )-Analogue d'aldéhyde de Garner, tert -butyl(3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylate
Hazmat
Documents
$119.48 /1G
Taille
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Product Information

(R)-N-Boc-1-oxa-4-azaspiro[4.5]decane-3-carboxaldehyde is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique spirocyclic structure that enhances its stability and reactivity, making it an excellent candidate for the development of novel pharmaceuticals and agrochemicals. Its distinctive functional groups allow for diverse modifications, facilitating the synthesis of complex molecules. Researchers appreciate its application in the preparation of biologically active compounds, particularly in the design of potential drug candidates targeting various diseases.

The compound's ability to serve as a building block in the synthesis of more complex structures is particularly valuable in the pharmaceutical industry. Its use in the development of spirocyclic derivatives has shown promise in enhancing the efficacy of therapeutic agents. Additionally, (R)-N-Boc-1-oxa-4-azaspiro[4.5]decane-3-carboxaldehyde is recognized for its potential in the synthesis of chiral intermediates, which are crucial for producing enantiomerically pure drugs. This compound stands out due to its unique structural features, offering researchers a reliable option for innovative chemical synthesis.

Synonyms
Ester 1,1-diméthyléthylique de l'acide (3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylique, ( R )-Analogue d'aldéhyde de Garner, tert -butyl(3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylate
CAS Number
171623-07-7
Purity
≥ 94% (CG)
Molecular Formula
C 14 H 23 NON 4
Molecular Weight
0
MDL Number
MFCD24849718
PubChem ID
85340984
Melting Point
53 - 58 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[ á]22/D = 69 ° (C = 1 dans le chloroforme)
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Ester 1,1-diméthyléthylique de l'acide (3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylique, ( R )-Analogue d'aldéhyde de Garner, tert -butyl(3 R )-3-formyl-1-oxa-4-azaspiro[4.5]décane-4-carboxylate
CAS Number
171623-07-7
Purity
≥ 94% (CG)
Molecular Formula
C 14 H 23 NON 4
Molecular Weight
0
MDL Number
MFCD24849718
PubChem ID
85340984
Melting Point
53 - 58 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[ á]22/D = 69 ° (C = 1 dans le chloroforme)
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(R)-N-Boc-1-oxa-4-azaspiro[4.5]decane-3-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of novel drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic chemistry for constructing complex molecular architectures, providing a versatile building block for researchers aiming to create diverse chemical entities.
  • Material Science: The compound can be used in the formulation of advanced materials, including polymers and coatings, enhancing properties such as durability and resistance to environmental factors.
  • Biochemistry Research: It plays a role in studying enzyme mechanisms and interactions, aiding researchers in understanding biological processes at a molecular level.
  • Agrochemical Applications: This chemical is explored for its potential use in developing agrochemicals, contributing to more effective pest control solutions while minimizing environmental impact.

Citations