BOC-L-GLU(ME)-OME
BOC-L-GLU(ME)-OME is a type of structurally typical, bifunctional-protected chiral amino acid derivative. Due to the protection of the amino group by Boc group and the protection of the two carboxyl groups by methylation, the reaction site is controllable, the stereoconfiguration is stable, and the solubility is excellent. It has become a key intermediate in the fields of peptide drugs, small molecule chemical drugs, asymmetric synthesis, and biological materials.
The application scenarios of BOC-L-GLU(ME)-OME are highly concentrated in the four directions of pharmaceutical synthesis, peptide preparation, fine chemicals, and chiral catalysis. At the same time, it has clear process precautions in storage, operation, and post-treatment, which directly affect the product yield, purity, and production safety.
Other supplier products
|
|
BOC-L-GLU(ME)-OME |
Boc-L-Glu(OMe)-OMe is a protected L-glutamic acid derivative (not a bioactive or therapeutic agent) with a single core mechanism of action: serving... |
|
|
L-Cysteine S-sulfate sodium salt |
L-Cysteine S-sulfate sodium salt, chemically namedsodium (2R)-2-amino-3-sulfonatosulfanylpropanoate, is a sulfur-containing amino acid derivative f... |
|
|
L-Cystine dihydrochloride powder |
Main Applications ofL-Cystine dihydrochloride
Cell Culture Media
Essential supplement for mammalian, insect, and microbial cell culture... |
|
|
Glycyl-glycine |
Glycyl-glycine is generally recognized as safe, with minimal side effects at typical supplemental doses. Its applications are most prominent in fo... |
|
|
L-Cysteine S-Sulfate Na |
Redox Properties of L-Cysteine S-Sulfate NaTheS-sulfonate-thiol linkage (-S-SO_3^-)is the core structural moiety responsible for the redox reactivi... |
供应产品
Same products