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734047

Sigma-Aldrich

(S)-3-Aminotetrahydrofuran tosylate

97%

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About This Item

Empirical Formula (Hill Notation):
C11H17NO4S
CAS Number:
104530-80-5
Molecular Weight:
259.32
MDL number:
MFCD00066238
UNSPSC Code:
12352005
PubChem Substance ID:
329764867
NACRES:
NA.22

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

SMILES string

N[C@H]1CCOC1.Cc2ccc(cc2)S(O)(=O)=O

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

InChI key

BZXPLADBSZWDIH-VWMHFEHESA-N

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.[1] It may also be used in the preparation of N-(4-fluoro-3-methyl-phenyl)-3-[[(3S)-tetrahydrofuran-3-yl]-sulfamoyl]benzamide derivatives.[2]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

734047-BULK:
734047-VAR:
734047-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBG2631V

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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)
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)

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