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Home  > 14-Azido-3,6,9,12-tetraoxatetradecan-1-ylamine

AI63970

951671-92-4 | 14-Azido-3,6,9,12-tetraoxatetradecan-1-ylamine

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $76.00 $54.00 -   +
5g 95% in stock $310.00 $217.00 -   +
10g 95% in stock $549.00 $384.00 -   +
25g 95% in stock $914.00 $640.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI63970
Chemical Name: 14-Azido-3,6,9,12-tetraoxatetradecan-1-ylamine
CAS Number: 951671-92-4
Molecular Formula: C10H22N4O4
Molecular Weight: 262.30608000000007
MDL Number: MFCD20134134
SMILES: NCCOCCOCCOCCOCCN=[N+]=[N-]

 

Computed Properties
Complexity: 212  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 14  
XLogP3: -0.4  

 

 

Upstream Synthesis Route
  • To synthesize 14-Azido-3,6,9,12-tetraoxatetradecan-1-ylamine, commence with the starting material of tetraethylene glycol. Protect the hydroxyl groups through a silylation reaction using tert-butyldimethylsilyl chloride (TBDMS-Cl) in the presence of imidazole as the base, and purify the resultant silyl ether.
    
    Next, conduct a mono-tosylation of the protected tetraethylene glycol using p-toluenesulfonyl chloride (TsCl) with a base such as triethylamine (Et3N) to yield the monotosylate, while keeping the reaction conditions mild enough to prevent ditosylation. Purify the monotosylated compound accordingly.
    
    Subsequently, replace the tosyl group with an azide group via nucleophilic substitution using sodium azide (NaN3) in a suitable solvent, such as dimethyl sulfoxide (DMSO), maintaining the temperature to prevent any potential decomposition of azide.
    
    Finally, remove the silyl protecting groups using an acid such as hydrochloric acid (HCl) in a mixture of tetrahydrofuran (THF) and water to obtain the desired 14-Azido-3,6,9,12-tetraoxatetradecan-1-ylamine. Purification can be performed through standard chromatographic techniques to yield the target compound at an appropriate level of purity for downstream applications.
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