CAS 165534-43-0
:Phosphate de diéthyle 4-oxo-1,2,3-benzotriazin-3-yle
- 1,2,3-Benzotriazin-4(3H)-one, 3-[(diethoxyphosphinyl)oxy]-
- 3-(Diethoxy-Phosphoryloxy)-3H-Benzo[D][1,2,3]Triazin-4-One
- 3-(Diethoxyphosphoryloxy)-1,2,3-Benzotriazin-4(3H)-One
- 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one (DEPBT)
- 3-Diethoxyphosphoryl-1,2,3-Benzotriazin-4(3H)-One
- 3-[(Diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one
- Depbt
- Depet
- Diethyl 3,4-Dihydro-4-Oxo-1,2,3-Benzotriazin-3-Yl Phosphate
- Diethyl 4-oxo-1,2,3-benzotriazin-3-yl phosphate
- Diethyl-(4-Oxo-3H-1,2,3-Benzotriazin-3-Yl)Phosphate
- Voir plus de synonymes
3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one
CAS :Formule :C11H14N3O5PDegré de pureté :>98.0%(HPLC)(N)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :299.223-Diethoxyphosphoryloxy-1,2,3-benzotriazin-4(3H)-one, 98%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo SciFormule :C11H14N3O5PDegré de pureté :98%Couleur et forme :Powder, WhiteMasse moléculaire :299.22DEPBT
CAS :DEPBT, a crystalline phosphonium-type coupling reagent, mediates amide bond formation with a remarkable resistance to racemization. Thus, DEPBT is an excellent activation reagent for coupling the racemization-prone Fmoc-His(Trt)-OH. The use of DEPBT permitted the total synthesis of the antiviral peptide antibiotic feglymycin, which contains a high proportion of ring-substituted phenylglycines.Formule :C11H14N3O5PCouleur et forme :WhiteMasse moléculaire :299.22Phosphoric acid, diethyl 4-oxo-1,2,3-benzotriazin-3-yl ester
CAS :Formule :C11H14N3O5PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :299.21973-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4-(3H)-one (DEPBT)
CAS :Formule :C11H14N3O5PMasse moléculaire :299.223-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one
CAS :3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneFormule :C11H14N3O5PDegré de pureté :98%Couleur et forme : white solidMasse moléculaire :299.22g/mol3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4-(3H)-one
CAS :Formule :C11H14N3O5PDegré de pureté :98%Couleur et forme :Solid, Crystalline or PowderMasse moléculaire :299.223DEPBT (3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one) extrapure, 98%
CAS :Formule :C11H14N3O5PDegré de pureté :min. 98.0%Couleur et forme :White to almost white, Powder to CrystalMasse moléculaire :299.22DEPBT
CAS :DEPBT is an organophosphorous coupling reagent used in peptide chemistry. DEPBT is efficient in the synthesis of linear, cyclic and sterically hindered peptides, in solution and solid phase synthesis, achieving high yields with fast kinetics and remarkable retention of configuration. DEPBT can be easily synthesised, is a crystalline phosphate stable for months and shows often better performances than the commonly used phosphonium and uronium salts. Notably, in presence of DEPBT it is not necessary to protect the hydroxyl group in the amino acids (such as tyrosine, serine, and threonine) and the imidazole group of histidine. Therefore, DEPBT can be employed in the synthesis of amino alcohols and N-glycopeptides. DEPBT finds application in the synthesis of numerous bioactive peptides and complex natural products.
Formule :C11H14N3O5PDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :299.22 g/mol









