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1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE, a chemical compound belonging to the class of thiophenes, is characterized by its cyclic sulfide structure with a dioxo functional group and a tetrahydro-thiophen ring. This unique combination of features endows it with versatile chemical and structural properties, making it a valuable component in various industrial applications.

17115-51-4

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17115-51-4 Usage

Uses

Used in Organic Chemical Production:
1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE is used as a key intermediate in the synthesis of various organic chemicals. Its presence in the molecular structure facilitates the formation of new compounds, contributing to the development of innovative materials and products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE is utilized as a building block for the development of new drugs. Its unique chemical properties allow for the creation of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Industry:
1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE is employed in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these products enhances their effectiveness in controlling pests and weeds, thereby improving crop yields and agricultural productivity.
Used in Materials Science:
In the field of materials science, 1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE serves as a valuable component in the synthesis of advanced materials. Its unique structural properties enable the development of new materials with improved performance characteristics, such as enhanced stability, durability, and functionality.
Used in Research and Development:
1,1-DIOXO-TETRAHYDRO-1LAMBDA6-THIOPHEN-3-ONE is also utilized in research and development efforts due to its distinctive chemical and structural properties. Scientists and researchers leverage its unique features to explore new avenues in chemical synthesis, material development, and potential applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17115-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,1 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17115-51:
(7*1)+(6*7)+(5*1)+(4*1)+(3*5)+(2*5)+(1*1)=84
84 % 10 = 4
So 17115-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O3S/c5-4-1-2-8(6,7)3-4/h1-3H2

17115-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Dihydrothiophen-3(2H)-one 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 1,1-dioxothiolan-3-one

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:17115-51-4 SDS

17115-51-4Downstream Products

17115-51-4Relevant academic research and scientific papers

A Convenient Multigram Scale Synthesis of Tetrahydrothiophene-3-one-1,1-dioxide

Altenbach, Robert J.,Kalvoda, Ladislav,Carroll, William A.

, p. 567 - 570 (2004)

A short and efficient multigram scale synthesis of tetrahydrothiophene-3-one-1,1-dioxide is described.

Merging Halogen-Atom Transfer (XAT) and Cobalt Catalysis to Override E2-Selectivity in the Elimination of Alkyl Halides: A Mild Route towardcontra-Thermodynamic Olefins

Zhao, Huaibo,McMillan, Alastair J.,Constantin, Timothée,Mykura, Rory C.,Juliá, Fabio,Leonori, Daniele

supporting information, p. 14806 - 14813 (2021/09/18)

We report here a mechanistically distinct tactic to carry E2-type eliminations on alkyl halides. This strategy exploits the interplay of α-aminoalkyl radical-mediated halogen-atom transfer (XAT) with desaturative cobalt catalysis. The methodology is high-yielding, tolerates many functionalities, and was used to access industrially relevant materials. In contrast to thermal E2 eliminations where unsymmetrical substrates give regioisomeric mixtures, this approach enables, by fine-tuning of the electronic and steric properties of the cobalt catalyst, to obtain high olefin positional selectivity. This unprecedented mechanistic feature has allowed access tocontra-thermodynamic olefins, elusive by E2 eliminations.

IMIDAZO [4, 5 -C] PYRIDINE DERIVATIVES USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES

-

Paragraph 00570, (2013/08/28)

Wherein R1, L1, R3, R4, Cy, L2 and R5 are as defined herein. Novel imidazolopyridines according to Formula I, able to inhibit JAK are disclosed, these compounds may be prepared as a pharmaceutical composition, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 or interferons.

Synthesis of cyclopentapyridine and thienopyridine derivatives as potential calcium channel modulators

Guenduez,Safak,Kaygsz,Kosar,Simsek,Erol,Linden

experimental part, p. 167 - 175 (2012/09/08)

In this study, novel condensed 1,4-dihydropyridines bearing cyclopentanone (1-21) or tetrahydrothiophene-1,1-dioxide ring (22-42) with various ester substituents were synthesized via a modified Hantzsch reaction and their calcium channel modulator activities were investigated on isolated rat ileum and rat thoracic aorta. The introduction of a cyclopentanone ring fused to the 1,4-dihydropyridine nucleus and methyl, ethyl and allyl moieties to the ester group led to more active calcium modulators. Georg Thieme Verlag KG Stuttgart · New York.

Synthesis and myorelaxant activity of fused 1,4-dihydropyridines on isolated rabbit gastric fundus

Safak, Cihat,Guenduez, Miyase Goezde,Oezlhan, Sevil Oezger,Simasek, Rahime,Is, Fatma,Yildirim, Seniz,Fincan, Goekce Sevim Oeztuerk,Saraoglu, Yusuf,Linden, Anthony

, p. 332 - 342 (2012/10/29)

Strategy, Management and Health Policy Preclinical Research In the present study, 25 novel condensed 1,4-dihydropyridine (DHP) derivatives bearing cyclopentane, cyclohexane, or tetrahydrothiopene ring with a bulky and lipophilic moiety (3-pyridylmethyl) in the ester group were synthesized via a modified Hantzsch reaction, and their calcium channel modulator activities were assayed on isolated rabbit gastric fundus smooth muscle strips. To evaluate the myorelaxant effects of the compounds, the maximum relaxant response (Emax) and pD 2 values were calculated. The results indicated that all compounds produced concentration-dependent relaxation and the introduction of five- or six-membered rings to the DHP nucleus and 3-pyridiylmethyl moiety to the ester group led to potent calcium antagonists.

Pyrano, piperidino, and thiopyrano compounds and methods of use

-

, (2008/06/13)

The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.

Pyrano, piperidino, and thiopyrano compounds and methods of use

-

, (2008/06/13)

The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.

Synthesis of Novel Cyclic Sulfone Dihydropyridines Facilitated by a Selective Ethyl Diazoacetate Ring Expansion

Dodd, John H.,Schwender, Charles F.,Gray-Nunez, Yolanda

, p. 1453 - 1456 (2007/10/02)

A series of novel cyclic sulfone dihydropyridines with five to nine membered rings have been synthesized.Anomalous intermediates isolated from the Hantzch condensation were found to vary depending on the sulfone ring size and aromatic substitution.Tin tetrachloride has been shown to be a superior Lewis acid catalyst for ethyl diazoacetate ring expansion of the requisite β-keto cyclic sulfone precursors.

3-OXOTETRAHYDROTHIOPHEN-1,1-DIOXIDE A VERSATILE SYNTHETIC INTERMEDIATE

Belletire, J. L.,Spletzer, E. G.

, p. 269 - 272 (2007/10/02)

An improved preparation and valuable new reactions of 3-oxotetrahydrothiophen-1,1-dioxide are described.

STEREOSPECIFIC SYNTHESIS OF ETHERS OF HYDROXYTETRAHYDROTHIOPHENE-1,1-DIOXIDES USING INTERPHASE CATALYSIS

Tolstikov, G. A.,Novitskaya, N. N.,Shul'ts, E. E.

, p. 1129 - 1134 (2007/10/02)

Methods have been developed for the stereospecific synthesis of O-benzyl- and O-methyl-derivatives of hydroxytetrahydrothiophene-1,1-dioxides in the presence of phase transfer catalysts.

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