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544479-61-0

2-(tert-butoxycarbonylaMino)-4,4,4-trifluorobutanoic acid

Catalog#: AR00DFYP  |   CAS#: 544479-61-0  |   MDL#: MFCD02682446  |   MF: C9H14F3NO4  |   MW: 257.2070

Packsize Purity Price Availability Quantity
250mg 95% $284.00 2-3 weeks Buy Now Add To Cart
500mg 95% $432.00 2-3 weeks Buy Now Add To Cart
1g 95% $547.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,171.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,210.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00DFYP
Chemical Name 2-(tert-butoxycarbonylaMino)-4,4,4-trifluorobutanoic acid
CAS Number 544479-61-0
Molecular Formula C9H14F3NO4
Molecular Weight 257.2070
MDL Number MFCD02682446
SMILES O=C(OC(C)(C)C)NC(C(=O)O)CC(F)(F)F

The compound 2-((tert-Butoxycarbonyl)amino)-4,4,4-trifluorobutanoic acid is a versatile building block in chemical synthesis. It is commonly used as a protecting group for the amino functionality in various organic reactions. This compound offers several key advantages in synthesis processes:1. Protection of Amino Groups: The tert-Butoxycarbonyl (Boc) protecting group on the amino functionality prevents unwanted reactions at this site during synthetic manipulations. This protection allows other functional groups in the molecule to undergo specific transformations without interference from the amino group.2. Selective Deprotection: The Boc group can be selectively removed under mild conditions, such as with acids or bases, to reveal the free amine for further modification. This controlled deprotection step adds flexibility and precision to the synthesis pathway.3. Compatibility with Fluorinated Molecules: The trifluorobutanoic acid moiety in this compound can also serve as a handle for introducing fluorine atoms into the target molecule. Fluorinated compounds are valuable in medicinal chemistry, agrochemicals, and materials science due to the unique properties conferred by fluorine substitution.4. Enhanced Solubility and Stability: The presence of the bulky tert-butyl group in the Boc protecting group can enhance the solubility and stability of the compound, making it easier to handle in various reaction conditions.Overall, 2-((tert-Butoxycarbonyl)amino)-4,4,4-trifluorobutanoic acid plays a crucial role in chemical synthesis by providing protection, selectivity, and functional group compatibility. Its utility in constructing complex molecules makes it a valuable tool for synthetic chemists in diverse research areas.
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