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4-AMINO-3-HYDROXYTETRAHYDROTHIOPHENE, 1,1-DIOXIDE is a versatile chemical compound featuring a tetrahydrothiophene ring with an amino group and a hydroxyl group, along with a 1,1-dioxide group. It is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as for its anti-inflammatory, antioxidant, antibacterial, and antifungal properties.

55261-00-2

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55261-00-2 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINO-3-HYDROXYTETRAHYDROTHIOPHENE, 1,1-DIOXIDE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and antioxidant properties. It aids in the development of drugs targeting a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINO-3-HYDROXYTETRAHYDROTHIOPHENE, 1,1-DIOXIDE is utilized as a building block in the creation of agrochemicals, leveraging its antibacterial and antifungal activities to protect crops and enhance agricultural productivity.
Used in Research and Development:
4-AMINO-3-HYDROXYTETRAHYDROTHIOPHENE, 1,1-DIOXIDE is employed as a subject of study in research for its potential therapeutic applications, including the development of new drugs and treatments based on its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 55261-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,6 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55261-00:
(7*5)+(6*5)+(5*2)+(4*6)+(3*1)+(2*0)+(1*0)=102
102 % 10 = 2
So 55261-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO3S/c5-3-1-9(7,8)2-4(3)6/h3-4,6H,1-2,5H2/t3-,4-/m0/s1

55261-00-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-3-hydroxytetrahydrothiophene, 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-3-aminosulfolane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55261-00-2 SDS

55261-00-2Relevant academic research and scientific papers

Kinase inhibitor compounds

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Page/Page column 20, (2009/04/24)

The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein can be used for the therapeutic modulation of kinase-mediated processes, and treatment of disease and disease symptoms, particularly those mediated by certain kinase enzymes.

KINASE INHIBITOR COMPOUNDS

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Page/Page column 47, (2008/06/13)

The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein can be used for the therapeutic modulation of kinase-mediated processes, and treatment of disease and disease symptoms, particularly those mediated by certain kinase enzymes.

Structure-activity studies of cyclic ketone inhibitors of the serine protease plasmin: Design, synthesis, and biological activity

Xue, Fengtian,Seto, Christopher T.

, p. 8467 - 8487 (2008/02/05)

Three series of cyclic ketone inhibitors were synthesized and evaluated against the serine protease plasmin. Peptide inhibitors that incorporated 3-oxotetrahydrofuran and 3-oxotetrahydrothiophene 1,1-dioxide groups had the highest activities. Alkylamino substituents, which were designed to bind in the S1 subsite of plasmin, were attached to the inhibitors. Compounds 5c and 5g, which incorporated 6-aminohexyl substituents, were found to be optimal and demonstrated IC50 values in the low micromolar range. Incorporating conformationally constrained peptide segments into the inhibitors did not improve their activities.

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