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BOC-MET-OH DCHA

  • Name BOC-MET-OH DCHA
  • CAS 22823-50-3
  • Purity 99%
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1.What is the BOC-MET-OH DCHA ?

BOC-MET-OH DCHA is a chemical compound that integrates a BOC (tert-butoxycarbonyl) protecting group, methionine (MET) amino acid, and DCHA (dicyclohexylamine) coupling reagent. BOC-MET-OH DCHA is designed for use in organic synthesis and peptide synthesis, where the BOC group shields amino groups, methionine serves as a fundamental building block of proteins, and DCHA facilitates the formation of amide bonds between amino acids, enabling the creation of peptides and proteins with tailored sequences and characteristics.

2.What is the CAS number for BOC-MET-OH DCHA ?

The CAS number of BOC-MET-OH DCHA is 22823-50-3.

3.What are another words for BOC-MET-OH DCHA ?

Synonyms?for?BOC-MET-OH DCHA 22823-50-3:BOC-MET-OH DCHA;Boc-Met-OH·DCHA;

4.What is BOC-MET-OH DCHA (22823-50-3) used for?

Used in Pharmaceutical Industry:
BOC-MET-OH DCHA is used as a key component in the synthesis of peptides and proteins for various pharmaceutical applications. Its role in protecting amino groups and aiding in the formation of amide bonds is crucial for the development of therapeutic peptides and proteins with specific biological activities.
Used in Biochemistry Research:
In biochemistry, BOC-MET-OH DCHA serves as a valuable tool for researchers studying protein structure and function. Its ability to facilitate the synthesis of peptides with specific sequences allows for the exploration of protein interactions and mechanisms at a molecular level.
Used in Peptide Synthesis:
BOC-MET-OH DCHA is used as a coupling agent in peptide synthesis to efficiently link amino acids together. This is essential for the production of custom peptides for use in drug discovery, diagnostics, and other applications where specific peptide sequences are required.
Used in Organic Synthesis:
Beyond its applications in peptide chemistry, BOC-MET-OH DCHA can also be utilized in broader organic synthesis processes. The BOC protecting group is particularly useful in protecting amino groups during reactions where such groups might otherwise interfere with the desired synthetic pathway.

InChI:InChI=1/C12H23N.C10H19NO4S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-10(2,3)15-9(14)11-7(8(12)13)5-6-16-4/h11-13H,1-10H2;7H,5-6H2,1-4H3,(H,11,14)(H,12,13)/t;7-/m.0/s1

Relevant articles related to BOC-MET-OH DCHA:

Article

Source

Peptide synthesis in aqueous solution. IV. Preparation and properties of [p-(benzyloxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate, [p-(t-butoxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate and [p-(9-fluorenylmethyl-oxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate as water-soluble N-acylating reagents

Azuse,Tamura,Kinomura,Okai,Kouge,Hamatsu,Koizumi

, p. 3103 - 3108 (2007/10/02)

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