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Home  > Chemistry  > Organic Building Blocks  > Aliphatic Chain Hydrocarbons  > 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide

AD44885

1076199-21-7 | 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $15.00 $10.00 -   +
250mg 95% in stock $17.00 $12.00 -   +
1g 95% in stock $38.00 $26.00 -   +
5g 95% in stock $161.00 $113.00 -   +
10g 95% in stock $288.00 $201.00 -   +
100g 95% in stock $2,219.00 $1,554.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD44885
Chemical Name: 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide
CAS Number: 1076199-21-7
Molecular Formula: C13H26BrNO5
Molecular Weight: 356.25323999999995
MDL Number: MFCD09840081
SMILES: BrCCOCCOCCOCCNC(=O)OC(C)(C)C

 

Computed Properties
Complexity: 245  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 13  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide is a versatile chemical compound commonly used in chemical synthesis. This compound serves as an important building block in organic chemistry due to its unique reactivity and structural characteristics. In chemical synthesis, 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide is used as a key intermediate for the preparation of various bioactive compounds, pharmaceuticals, and other complex molecules. Its bromide functionality enables easy derivatization and further conversion into a wide range of functionalized products. Additionally, the Boc (tert-butoxycarbonyl) protecting group on the amino moiety provides stability and selective reactivity, making it a valuable tool for controlling the regioselectivity and stereochemistry of chemical reactions.Overall, the application of 1-Boc-amino-3,6,9-trioxaundecanyl-11-bromide in chemical synthesis exemplifies its significance in the construction of intricate molecular architectures and the development of new compounds with potential biological activities.
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