(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one

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(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
EINECS:
Product Categories:
Mol File:173401-47-3.mol
(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one Structure
(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
pka13.90±0.40(Predicted)
color White to off-white
Safety Information
MSDS Information
(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one Usage And Synthesis
UsesNorbiotinamine 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 ofNorbiotinamineand 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)-one Preparation Products And Raw materials
Tag:(3aS,4S,6aR)-4-(4-aminobutyl)tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-one(173401-47-3) Related Product Information
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