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  • Fmoc-Asp(OBzl)-OH CAS:86060-84-6

    Fmoc-Asp(OBzl)-OH CAS:86060-84-6

    Fmoc-Asp(OBzl)-OH, or Fmoc-aspartic acid with benzyl (OBzl) protection, is a pivotal component in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the aspartic acid molecule, with an additional benzyl group safeguarding the carboxyl group. Fmoc-Asp(OBzl)-OH is renowned for its role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the aspartic acid carboxyl group.

  • Fmoc-Asn-OH CAS:71989-16-7

    Fmoc-Asn-OH CAS:71989-16-7

    Fmoc-Asn-OH, or Fmoc-asparagine, is a vital component in peptide synthesis, featuring a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the asparagine molecule. Widely utilized in both solid-phase and solution-phase peptide synthesis, this derivative selectively shields the amino group of asparagine, facilitating controlled peptide chain elongation. Fmoc-Asn-OH is recognized for its compatibility with various coupling reagents and solid supports, making it a cornerstone in the field of peptide chemistry.

  • FmFmoc-Asp-OBut CAS:129460-09-9

    FmFmoc-Asp-OBut CAS:129460-09-9

    Fmoc-Asp-OBut, or Fmoc-aspartic acid with O-butyl (OBut) protection, is a significant compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the aspartic acid molecule, with an additional O-butyl group safeguarding the carboxyl group. Fmoc-Asp-OBut plays a crucial role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the aspartic acid carboxyl group.

  • Fmoc-Arg(Tos)-OH CAS:83792-47-6

    Fmoc-Arg(Tos)-OH CAS:83792-47-6

    Fmoc-Arg(Tos)-OH, or Fmoc-arginine with tosyl (Tos) protection, is a key derivative employed in peptide synthesis. Featuring a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the arginine molecule, with an additional tosyl group on the guanidine nitrogen, this compound offers enhanced selectivity during peptide chain elongation. Fmoc-Arg(Tos)-OH is notable for its specialized role in peptide chemistry, where the dual protection strategy facilitates controlled manipulation of the guanidine nitrogen’s reactivity.

  • Fmoc-D-Asn(Trt)-OH CAS:180570-71-2

    Fmoc-D-Asn(Trt)-OH CAS:180570-71-2

    Fmoc-D-Asn(Trt)-OH, or Fmoc-D-asparagine with trityl (Trt) protection, is a pivotal component in peptide synthesis. This derivative comprises a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the D-enantiomer of asparagine, with an additional trityl group guarding the amino group. Fmoc-D-Asn(Trt)-OH holds significance in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the D-asparagine amino group.

     

  • Fmoc-Asp(OBut)-OH CAS:71989-14-5

    Fmoc-Asp(OBut)-OH CAS:71989-14-5

    Fmoc-Asp(OBut)-OH, or Fmoc-aspartic acid with O-butyl (OBut) protection, is a key component in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the aspartic acid molecule, with an additional O-butyl group safeguarding the carboxyl group. Fmoc-Asp(OBut)-OH plays a crucial role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the aspartic acid carboxyl group.

  • Fmoc-Asp(OBut)-OSu CAS:78553-23-8

    Fmoc-Asp(OBut)-OSu CAS:78553-23-8

    Fmoc-Asp(OBut)-OSu, or Fmoc-aspartic acid with O-butyl (OBut) protection and N-hydroxysuccinimide (OSu) ester functionality, is a pivotal compound in peptide synthesis. This derivative features a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group attached to the aspartic acid molecule, with an additional O-butyl group safeguarding the carboxyl group and an OSu ester group facilitating efficient coupling reactions. Fmoc-Asp(OBut)-OSu plays a crucial role in peptide chemistry, offering enhanced selectivity during peptide chain elongation and controlled manipulation of the aspartic acid carboxyl group.

  • Fmoc-Asn(Trt)-OH CAS:132388-59-1

    Fmoc-Asn(Trt)-OH CAS:132388-59-1

    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.

  • o-Methyl-N-Acetoacetanilide CAS:93-68-5

    o-Methyl-N-Acetoacetanilide CAS:93-68-5

    o-Methyl-N-Acetoacetanilide, with the chemical formula C11H13NO3, is a crystalline compound known for its distinctive properties. This organic compound is utilized in various industrial applications due to its unique chemical structure and reactivity.

  • Ethyl4-methyl-1,2,3-thiadiazole-5-carboxylate  CAS:18212-20-9

    Ethyl4-methyl-1,2,3-thiadiazole-5-carboxylate CAS:18212-20-9

    Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate is a chemical compound represented by the molecular formula C7H8N2O2S. This compound falls into the category of thiadiazole derivatives, featuring a unique structure with a methyl group and a carboxylate moiety. Known for its diverse applications, it is a valuable component in various chemical processes.

  • N,N-Dimethylallylamine CAS:2155-94-4

    N,N-Dimethylallylamine CAS:2155-94-4

    N,N-Dimethylallylamine, with the chemical formula C6H13N, is a clear liquid characterized by its distinctive properties. This organic compound is widely used in various industrial applications due to its unique chemical structure and reactivity.

  • o-Acetoacetaniside CAS:92-15-9

    o-Acetoacetaniside CAS:92-15-9

    o-Acetoacetaniside, with the chemical formula C10H11NO4, is a crystalline compound known for its distinctive properties. This organic compound is employed in various industrial applications due to its unique chemical structure and reactivity.