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200124-22-7

L-Ornithine, N5-[[[(2,3-dihydro-2,2,4,6,7-pentamethyl-5-benzofuranyl)sulfonyl]amino]iminomethyl]-N2-[(1,1-dimethylethoxy)carbonyl]-

Catalog#: AR002D8V  |   CAS#: 200124-22-7  |   MDL#: MFCD00236821  |   MF: C24H38N4O7S  |   MW: 526.6461199999998

Packsize Purity Price Availability Quantity
250mg 95% $4.00 Global Stock Buy Now Add To Cart
1g 95% $4.00 Global Stock Buy Now Add To Cart
5g 95% $7.00 Global Stock Buy Now Add To Cart
25g 95% $30.00 Global Stock Buy Now Add To Cart
100g 95% $119.00 Global Stock Buy Now Add To Cart
500g 95% $595.00 Global Stock Buy Now Add To Cart
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Catalog Number AR002D8V
Chemical Name L-Ornithine, N5-[[[(2,3-dihydro-2,2,4,6,7-pentamethyl-5-benzofuranyl)sulfonyl]amino]iminomethyl]-N2-[(1,1-dimethylethoxy)carbonyl]-
CAS Number 200124-22-7
Molecular Formula C24H38N4O7S
Molecular Weight 526.6461199999998
MDL Number MFCD00236821
SMILES O=C(OC(C)(C)C)N[C@H](C(=O)O)CCCNC(=N)NS(=O)(=O)c1c(C)c(C)c2c(c1C)CC(O2)(C)C

Boc-Arg(Pbf)-OH, also known as N-alpha-butoxycarbonyl-L-arginyl-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-arginine, is a key reagent commonly used in chemical synthesis. This compound is utilized as a protected form of the amino acid arginine, offering a range of applications in organic chemistry.In peptide synthesis, Boc-Arg(Pbf)-OH serves as a versatile building block for the creation of larger peptides and proteins. The Boc (tert-butyloxycarbonyl) protecting group shields the amino group on the arginine residue, enabling selective deprotection and subsequent coupling reactions. The Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group safeguards the guanidine moiety of arginine, preventing unwanted side reactions. This dual protection strategy ensures the controlled assembly of complex peptide sequences.Furthermore, Boc-Arg(Pbf)-OH finds utility in the synthesis of pharmaceuticals, natural products, and peptidomimetics. Its compatibility with solid-phase peptide synthesis techniques makes it a valuable tool for drug discovery and development. By incorporating Boc-Arg(Pbf)-OH into peptide precursors, chemists can construct bioactive molecules with improved stability and bioavailability.Overall, the strategic incorporation of Boc-Arg(Pbf)-OH in chemical synthesis enables precise control over peptide bond formation and functional group protection, facilitating the efficient production of diverse molecular architectures for various scientific and industrial applications.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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