734047
(S)-3-Aminotetrahydrofuran tosylate
97%
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About This Item
Empirical Formula (Hill Notation):
C11H17NO4S
CAS Number:
Molecular Weight:
259.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Product Name
(S)-3-Aminotetrahydrofuran tosylate, 97%
InChI
1S/C7H8O3S.C4H9NO/c1-6-2-4-7(5-3-6)11(8,9)10;5-4-1-2-6-3-4/h2-5H,1H3,(H,8,9,10);4H,1-3,5H2/t;4-/m.0/s1
SMILES string
N[C@H]1CCOC1.Cc2ccc(cc2)S(O)(=O)=O
InChI key
BZXPLADBSZWDIH-VWMHFEHESA-N
assay
97%
form
solid
optical activity
[α]22/D −4.5°, c = 0.5 in methanol
mp
133-138 °C
storage temp.
2-8°C
Application
(S)-3-Aminotetrahydrofuran tosylate can be used as a reagent in the synthesis of oxadiazolyl-quinolinyl-N-(pyranyl)piperidinamines as potential κ-opioid receptor (KOR) antagonists. It may also be used in the preparation of N-(4-fluoro-3-methyl-phenyl)-3-[[(3S)-tetrahydrofuran-3-yl]-sulfamoyl]benzamide derivatives.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Design and synthesis of a novel and selective kappa opioid receptor (KOR) antagonist (BTRX-335140)
Guerrero M, et al.
Journal of Medicinal Chemistry, 61(14), 6247-6260 (2019)
Synthesis and evaluation of N-phenyl-3-sulfamoyl-benzamide derivatives as capsid assembly modulators inhibiting hepatitis B virus (HBV)
Vandyck K, et al.
Journal of medicinal chemistry, 61(14), 6247-6260 (2018)
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