AA14603
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.
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 |
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 |
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.