Peptide Synthesis Reagents
Items 271 to 278 of 278 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fmoc-Ser(tBu)-OH | 71989-33-8 | sc-235202 | 10 g | $82.00 | ||
Fmoc-Ser(tBu)-OH serves as a versatile intermediate in peptide synthesis, characterized by its t-butyl protecting group that imparts stability and solubility. The Fmoc moiety allows for selective deprotection under mild conditions, streamlining the synthesis process. Its hydroxyl functionality can participate in intramolecular hydrogen bonding, which may affect the conformation and folding of peptides. This compound's reactivity and solubility profile enhance coupling efficiency, making it a valuable asset in synthetic strategies. | ||||||
Fmoc-N-Me-Aib-OH | 400779-65-9 | sc-493278A sc-493278B sc-493278 sc-493278C | 100 mg 250 mg 1 g 5 g | $67.00 $123.00 $244.00 $982.00 | ||
Fmoc-N-Me-Aib-OH is a distinctive amino acid derivative that features a bulky Fmoc group, which significantly impacts steric effects and enhances the stability of peptide chains during synthesis. The N-methyl substitution modifies the electronic environment, influencing the compound's reactivity and selectivity in coupling reactions. Its unique side chain facilitates the formation of diverse peptide structures, enabling the exploration of various conformational landscapes and interaction profiles. | ||||||
Fmoc-L-β-HPhe-OH | 193954-28-8 | sc-285768 sc-285768A | 1 g 5 g | $285.00 $1140.00 | ||
Fmoc-L-β-HPhe-OH is an intriguing amino acid derivative notable for its Fmoc protection, which facilitates selective deprotection during peptide synthesis. The compound's unique β-position introduces a distinct spatial arrangement, influencing the conformational dynamics of peptides. Its hydrophobic aromatic side chain enhances aggregation tendencies, while the chiral nature promotes specific interactions in coupling reactions, ultimately affecting the efficiency and yield of peptide synthesis processes. | ||||||
Fmoc-1,2-trans-ACHC-OH | 381241-08-3 | sc-294707B sc-294707 sc-294707A | 250 mg 1 g 5 g | $92.00 $199.00 $797.00 | ||
Fmoc-1,2-trans-ACHC-OH is a key reagent in peptide synthesis, characterized by its unique ability to stabilize reactive intermediates through intramolecular hydrogen bonding. This compound exhibits a distinct conformational flexibility, which can influence the orientation of side chains during coupling reactions. Its selective reactivity allows for the formation of complex peptide structures while minimizing side reactions, making it an essential tool for achieving high purity in synthetic pathways. | ||||||
Boc-4-phenyl-L-β-homophenylalanine | 332062-06-3 | sc-285110 sc-285110A | 250 mg 1 g | $440.00 $880.00 | ||
Boc-4-phenyl-L-β-homophenylalanine is a versatile amino acid derivative notable for its protective Boc (tert-butyloxycarbonyl) group, which facilitates selective deprotection during peptide synthesis. Its unique β-homophenylalanine structure introduces steric and electronic variations that influence peptide folding and stability. The phenyl substituent enhances π-π stacking interactions, promoting specific conformations in peptide chains, while its hydrophobic characteristics can modulate solubility and aggregation behavior in synthetic environments. | ||||||
Boc-4-trifluoromethyl-D-β-homophenylalanine | 269726-77-4 | sc-293689 sc-293689A | 250 mg 1 g | $315.00 $638.00 | ||
Boc-4-trifluoromethyl-D-β-homophenylalanine features a distinctive trifluoromethyl moiety that significantly modifies its steric and electronic characteristics, leading to enhanced solubility in organic solvents. This compound's unique structure facilitates specific interactions during peptide coupling, potentially accelerating reaction rates. The presence of the D-stereoisomer contributes to unique conformational dynamics, influencing the overall stability and folding behavior of synthesized peptides, thereby affecting their structural integrity. | ||||||
Fmoc-L-MeAsp(tBu)-OH | 152548-66-8 | sc-285783 sc-285783A | 1 g 5 g | $133.00 $473.00 | ||
Fmoc-L-MeAsp(tBu)-OH is a specialized amino acid derivative that features a tert-butyl group, which introduces notable steric hindrance, affecting the spatial arrangement during peptide assembly. The Fmoc group not only provides protection but also enhances the compound's solubility in organic solvents, promoting efficient coupling reactions. Its unique side chain fosters specific interactions, influencing reaction kinetics and enabling precise control over peptide chain elongation and folding. | ||||||
2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline | 16357-59-8 | sc-254228 sc-254228A | 5 g 25 g | $26.00 $49.00 | ||
2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline is a unique compound in peptide synthesis, notable for its ability to facilitate selective coupling reactions. Its ethoxycarbonyl group enhances nucleophilicity, promoting efficient amide bond formation. The dihydroquinoline structure introduces distinct steric and electronic properties, influencing reaction kinetics and selectivity. Additionally, its solubility characteristics support diverse reaction conditions, making it a flexible choice for complex peptide assembly. | ||||||