(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one
(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one Basic information
- Product Name:
- (3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one
- Synonyms:
-
- (3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one
- Norbiotinamine
- 1H-Thieno[3,4-d]imidazol-2(3H)-one, 4-(4-aminobutyl)tetrahydro-, (3aS,4S,6aR)-
- CAS:
- 173401-47-3
- MF:
- C9H17N3OS
- MW:
- 215.32
- Mol File:
- 173401-47-3.mol
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(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one Chemical Properties
- Boiling point:
- 478.0±30.0 °C(Predicted)
- Density
- 1.162±0.06 g/cm3(Predicted)
- storage temp.
- 4°C, protect from light
- solubility
- H2O : 200 mg/mL (928.85 mM; ultrasonic and warming and heat to 60°C)
- form
- Solid
- pka
- 13.90±0.40(Predicted)
- color
- White to off-white
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(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one Usage And Synthesis
Uses
Norbiotinamine is an alternative to biotin. Norbiotinamine can be coupled with a carboxylic group of amino acids to give inverse peptides, having the amide linkage oriented in the opposite direction[1].
References
[1] Szalecki W.Synthesis of?Norbiotinamine?and its derivatives. Bioconjug Chem.?1996 Mar-Apr;7(2):271-3. DOI:10.1021/bc950094f
[2] Zhou GC,?et al. Design, synthesis and evaluation of a cellular stable and detectable biotinylated fumagillin probe and investigation of cell permeability of fumagillin and its analogs to endothelial and cancer cells.Eur J Med Chem.?2013;70:631-9. DOI:10.1016/j.ejmech.2013.10.033
(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-oneSupplier
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