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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.
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Fmoc-MeGly-OH CAS:77128-70-2
Fmoc-MeGly-OH is a high-quality, protected form of N-methyl glycine, commonly known as sarcosine, utilized in peptide synthesis. This product features the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group on the amino terminus, ensuring stability during peptide assembly. With its exceptional purity and consistent quality, Fmoc-MeGly-OH serves as an essential building block for the efficient and reliable synthesis of diverse peptides, including those with modified backbone structures.
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Fmoc-Cys(But)-OH CAS:67436-13-9
Fmoc-Cys(But)-OH, or Fmoc-cysteine with butyl (But) protection, is a pivotal compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the cysteine molecule, with an additional butyl group safeguarding the thiol functionality. Fmoc-Cys(But)-OH plays a crucial role in peptide chemistry, providing enhanced selectivity during peptide chain elongation and controlled manipulation of the cysteine thiol group.
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Fmoc-Glu(OBzl)-OH CAS:123639-61-2
Fmoc-Glu(OBzl)-OH, or Fmoc-glutamic acid with benzyl (OBzl) protection, is a crucial component in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the glutamic acid molecule, with an additional benzyl group safeguarding the carboxyl group. Fmoc-Glu(OBzl)-OH plays a pivotal role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the glutamic acid carboxyl group.
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Fmoc-Asp(OcHx)-OH CAS:130304-80-2
Fmoc-Asp(OcHx)-OH, or Fmoc-aspartic acid with octyl (OcHx) protection, is a vital compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the aspartic acid molecule, with an additional octyl group safeguarding the carboxyl group. Fmoc-Asp(OcHx)-OH plays a crucial role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the aspartic acid carboxyl group.
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Fmoc-D-Asn-OH CAS:108321-39-7
Fmoc-D-Asn-OH, or Fmoc-D-asparagine, is a significant derivative in peptide synthesis, featuring a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the D-enantiomer of asparagine. This compound plays a pivotal role in solid-phase and solution-phase peptide synthesis, selectively protecting the amino group of D-asparagine for controlled peptide chain elongation. Fmoc-D-Asn-OH is recognized for its compatibility with various coupling reagents and solid supports, contributing to its importance in the realm of peptide chemistry.
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Fmoc-D-Asp(OBut)-OH CAS:112883-39-3
Fmoc-D-Asp(OBut)-OH, or Fmoc-D-aspartic acid with O-butyl (OBut) protection, is a crucial compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the D-enantiomer of aspartic acid, with an additional O-butyl group safeguarding the carboxyl group. Fmoc-D-Asp(OBut)-OH plays a pivotal role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the D-aspartic acid carboxyl group.
