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2-(2-BROMOACETYL)THIOPHENE CAS:10531-41-6
2-(2-Bromoacetyl)thiophene is a chemical compound belonging to the thiophene family, containing a bromoacetyl group. It is commonly used in organic synthesis and pharmaceutical research due to its unique properties and structural features.
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Fmoc-Gly-Cl CAS:103321-49-9
Fmoc-Gly-Cl is a high-quality, activated form of glycine featuring the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group and a reactive chloroacetyl functionality. This product is designed for efficient coupling with amino groups in peptide synthesis, enabling the introduction of glycine at specific positions within peptide sequences. With its exceptional purity and reactivity, Fmoc-Gly-Cl serves as a valuable tool for the precise and controlled modification of peptides.
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Fmoc-Gly-OH CAS:29022-11-5
Fmoc-Gly-OH is a premium-grade, protected form of glycine widely employed in peptide synthesis. This product incorporates the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, ensuring stability during peptide assembly and enabling facile deprotection. With its exceptional purity and consistency, Fmoc-Gly-OH serves as a fundamental building block for the efficient and reliable synthesis of diverse peptides.
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Fmoc-D-Gln-OH CAS:71989-20-3
Fmoc-D-Gln-OH, or Fmoc-D-glutamine, is a pivotal component in peptide synthesis. This compound features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the D-enantiomer of glutamine. Fmoc-D-Gln-OH plays a crucial role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the glutamine side chain in its D-form.
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Fmoc-Gly-OSu CAS:113484-74-5
Fmoc-Gly-OSu is a high-quality, activated form of glycine featuring the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group and the N-hydroxysuccinimide (NHS) ester functionality. This product is designed for efficient coupling with amino groups in peptide synthesis, enabling the introduction of glycine at specific positions within peptide sequences. With its exceptional purity and reactivity, Fmoc-Gly-OSu serves as a valuable tool for the precise and controlled modification of peptides.
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Fmoc-Gln(Trt)-OH CAS:132327-80-1
Boc-MeVal-OH is a crucial chemical compound widely used in peptide synthesis and pharmaceutical research. With a molecular formula of C11H21NO4, this product is highly valued for its high purity and reliability, serving as an essential component for producing specific peptide compounds in laboratory settings. Boc-MeVal-OH plays a significant role in organic synthesis, particularly in the amidation and deprotection steps involved in peptide assembly. Its stability and quality make it a valuable tool for researchers and scientists working on drug discovery and development, contributing to advancements in pharmaceuticals and biochemical studies.
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Fmoc-Glu(But)-NH2 CAS:104090-92-8
Fmoc-Glu(But)-NH2, or Fmoc-glutamic acid with butyl (But) protection and an amino group (NH2), is a significant compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the glutamic acid molecule, with an additional butyl group safeguarding the carboxyl group. The presence of the amino group adds versatility for downstream peptide modifications, making Fmoc-Glu(But)-NH2 a valuable building block in peptide chemistry.
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Fmoc -Glu(OcHx)-OH CAS:150047-85-1
Fmoc-Glu(OcHx)-OH, or Fmoc-glutamic acid with cyclohexyl (OcHx) protection, is a pivotal component in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the glutamic acid molecule, with an additional cyclohexyl group safeguarding the carboxyl group. Fmoc-Glu(OcHx)-OH plays a crucial role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the glutamic acid carboxyl group.
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Fmoc-Gln-OH CAS:118609-68-0
Fmoc-Gln-OH, or Fmoc-glutamine, is a key component in peptide synthesis. This compound features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the glutamine molecule. Fmoc-Gln-OH plays a crucial role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the glutamine side chain.
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Fmoc -Glu(OBut)-OSu CAS:101214-22-6
Fmoc-Glu(OBut)-OSu is a significant compound in peptide synthesis. This derivative of glutamic acid features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the amino group, with an additional butyl group safeguarding the carboxyl group, and activated as an N-hydroxysuccinimide ester. Fmoc-Glu(OBut)-OSu facilitates peptide conjugation reactions by reacting with primary amines, enabling efficient peptide coupling with amine-containing molecules or surfaces.
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Fmoc-Glu(OBut)-OH CAS:71989-18-9
Fmoc-Glu(OBut)-OH, or Fmoc-glutamic acid with butyl (OBut) protection, is a key component in peptide synthesis. This compound features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the glutamic acid molecule, with an additional butyl group safeguarding the carboxyl group. Fmoc-Glu(OBut)-OH plays a vital role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the glutamic acid carboxyl group.
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Fmoc-D-Cys(Trt)-OH CAS:167015-11-4
Fmoc-D-Cys(Trt)-OH, or Fmoc-D-cysteine with trityl (Trt) protection, is a critical compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the D-enantiomer of cysteine, with an additional trityl group safeguarding the thiol functionality. Fmoc-D-Cys(Trt)-OH plays a pivotal role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the D-cysteine thiol group.
