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Home  > tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

AA68004

1415841-82-5 | tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $22.00 $15.00 -   +
1g 97% in stock $49.00 $35.00 -   +
5g 97% in stock $127.00 $89.00 -   +
10g 97% in stock $249.00 $175.00 -   +
15g 97% in stock $337.00 $236.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA68004
Chemical Name: tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate
CAS Number: 1415841-82-5
Molecular Formula: C10H16BrNO2
Molecular Weight: 262.1435
MDL Number: MFCD28054768
SMILES: BrC1=CCCN(C1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 255  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 2  
XLogP3: 2.2  

 

 

Upstream Synthesis Route
  • The tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate is a versatile compound commonly utilized in chemical synthesis as a valuable building block. This compound can serve as a key intermediate in the creation of various organic compounds due to its unique structure and reactivity. In particular, it is often employed in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its presence in a synthetic route can enable the introduction of specific functionalities or structural motifs into the final target molecule, enhancing its properties or efficacy. Furthermore, the tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate can participate in various chemical transformations such as nucleophilic substitution, oxidative coupling, or cyclization reactions, expanding its utility in organic synthesis. Its strategic incorporation in the synthesis of complex molecules highlights its significance as a valuable tool for chemists in achieving their desired molecular designs.
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