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CAS 154970-45-3

tert-Butyl 5-Norbornene-2-carboxylate (endo- and exo- mixture) TCI B4267

tert-Butyl 5-Norbornene-2-carboxylate (endo- and exo- mixture) TCI B4267

Chemical Identity

CAS No.
154970-45-3
PubChem
CID 15607334·SID 253660239
Formula
C12H18O2
Molecular weight
194.27 g/mol
Purity
>95.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl bicyclo[2.2.1]hept-5-ene-2-carboxylate
SMILES
CC(C)(C)OC(=O)C1CC2CC1C=C2
InChIKey
BZBMBZJUNPMEBD-UHFFFAOYSA-N
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Tert-Butyl 5-Norbornene-2-carboxylate is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a building block in organic chemistry, it plays a crucial role in the development of advanced chemical structures. Its unique molecular structure allows for specific chemical reactions under various conditions, making it a versatile tool in synthetic chemistry. This compound is particularly valuable for researchers aiming to create new compounds or test chemical reactions in controlled environments.

The compound's stability under certain conditions, combined with its reactivity in specific environments, makes it a preferred choice for laboratory applications. Its ability to participate in substitution, coupling, and ring-opening reactions enhances its utility in organic synthesis. The tert-butyl group provides additional control over reactivity and stability, which is essential for precise chemical manipulations. This feature is especially important in research settings where accuracy and reproducibility are critical.

In Indonesian laboratories, Tert-Butyl 5-Norbornene-2-carboxylate is commonly used by chemists for the development of new compounds, testing chemical reactions, and producing industrial raw materials. Due to its specific properties and broad applications, it is a key component in research and development activities across various educational and research institutions in Indonesia.

TCI brochures (PDF)

  • Organic synthesis of complex molecules due to its reactivity and structural versatility in ring-opening and coupling reactions.
  • Development of new chemical compounds for pharmaceutical and industrial applications because of its stability and controlled reactivity.
  • Testing of chemical reactions under controlled laboratory conditions to study reaction mechanisms and outcomes.
  • Production of industrial raw materials through synthetic pathways that require precise chemical intermediates.
  • Research in chemical engineering and materials science for the creation of advanced polymers and functional materials.

Brand TCI
CAS number 154970-45-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid depending on the specific formulation
Storage Store in a cool, dry place away from direct sunlight and moisture

Tert-Butyl 5-Norbornene-2-carboxylate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and goggles. Storage should be away from incompatible substances to avoid any potential chemical interactions. Regular monitoring of storage conditions ensures the integrity of the compound remains intact for laboratory use.

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