logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Spiroes  > tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate

AA14603

1160247-29-9 | tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $83.00 $59.00 -   +
250mg 97% in stock $127.00 $89.00 -   +
1g 97% in stock $397.00 $278.00 -   +
10g 97% in stock $3,898.00 $2,729.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA14603
Chemical Name: tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate
CAS Number: 1160247-29-9
Molecular Formula: C17H21BrN2O3
Molecular Weight: 381.2642
MDL Number: MFCD12198582
SMILES: Brc1ccc2c(c1)NC(=O)C12CCN(CC1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 495  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.7  

 

 

Upstream Synthesis Route
  • The tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate compound plays a key role in chemical synthesis procedures, particularly in the realm of organic chemistry. Known for its versatile reactivity and structural composition, this compound is utilized as a valuable building block for the creation of complex organic molecules and pharmaceutical intermediates.In chemical synthesis, tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate serves as a crucial starting material for the construction of diverse molecular structures through various synthetic methodologies such as acylation, alkylation, and cyclization reactions. Its unique spirocyclic structure provides a solid foundation for the formation of intricate molecular frameworks, making it an indispensable tool for chemists engaged in the design and synthesis of novel compounds.Additionally, tert-Butyl 6-bromo-2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate exhibits high stability and compatibility with a wide range of reaction conditions, allowing for efficient and controlled transformations during chemical synthesis processes. Its presence in the toolkit of synthetic chemists enables the development of advanced synthetic routes and the access to a diverse array of functionalized compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.
FEATURED PRODUCTS