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(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide is a chemical compound characterized by the molecular formula C11H12OS and a molecular weight of 192.28 g/mol. It is a yellow to brown liquid with a molecular structure that features a thiophene ring and a phenyl group. (2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide is known for its applications in various fields, including organic synthesis, pharmaceutical research, and the production of drugs and agrochemicals. Additionally, it holds potential for the development of new materials and as a reagent in chemical reactions.

24463-88-5

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24463-88-5 Usage

Uses

Used in Organic Synthesis:
(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide serves as a valuable intermediate in organic synthesis, contributing to the formation of complex organic molecules and facilitating various chemical reactions.
Used in Pharmaceutical Research:
In pharmaceutical research, (2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide is utilized for the development and synthesis of new drug candidates, potentially leading to the discovery of novel therapeutic agents.
Used in Drug Production:
(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide plays a role in the production of drugs, where it may be incorporated into the molecular structure of pharmaceuticals, enhancing their efficacy and pharmacological properties.
Used in Agrochemicals:
(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide is also applied in the agrochemical industry, where it may be used in the synthesis of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Material Development:
(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide has potential applications in the development of new materials, where its unique structure and properties can be harnessed to create innovative and improved materials for various industries.
Used as a Reagent in Chemical Reactions:
(2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide functions as a reagent in various chemical reactions, enabling specific transformations and acting as a catalyst in certain processes.
It is important to handle and store (2E)-2-(phenylmethylidene)tetrahydrothiophene 1,1-dioxide with care, adhering to the appropriate safety precautions and guidelines to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 24463-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24463-88:
(7*2)+(6*4)+(5*4)+(4*6)+(3*3)+(2*8)+(1*8)=115
115 % 10 = 5
So 24463-88-5 is a valid CAS Registry Number.

24463-88-5SDS

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 (2E)-2-benzylidenethiolane 1,1-dioxide

1.2 Other means of identification

Product number -
Other names -

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:24463-88-5 SDS

24463-88-5Downstream Products

24463-88-5Relevant academic research and scientific papers

(: Z)-Tetrahydrothiophene and (Z)-tetrahydrothiopyran synthesis through nucleophilic substitution and intramolecular cycloaddition of alkynyl halides and EtOCS2K

Luo, Xianglin,Li, Yibiao,Chen, Xiuwen,Song, Zhiyan,Liang, Junyi,Liao, Chunshu,Zhu, Zhongzhi,Chen, Lu

, p. 7315 - 7319 (2019/08/15)

This protocol provides a novel, environmentally friendly and simple method for the synthesis of (Z)-tetrahydrothiophene derivatives using the nucleophilic thiyl radical intramolecular cycloaddition cascade process to construct C-S bonds under transition-m

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