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4-(TERT-BUTYLSULFANYL)BENZENECARBALDEHYDE, a member of the aldehyde class, is a yellow liquid with a molecular formula of C11H14OS and a molecular weight of 198.30 g/mol. Characterized by its reactivity and functional group, 4-(TERT-BUTYLSULFANYL)BENZENECARBALDEHYDE serves as a versatile building block in organic chemistry. The presence of the tert-butylsulfanyl group imparts stability and steric hindrance, influencing its reactivity and selectivity in various chemical reactions.

88357-16-8

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88357-16-8 Usage

Uses

Used in Pharmaceutical Industry:
4-(TERT-BUTYLSULFANYL)BENZENECARBALDEHYDE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(TERT-BUTYLSULFANYL)BENZENECARBALDEHYDE is utilized as an intermediate in the production of agrochemicals, playing a crucial role in the synthesis of various pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Chemistry:
4-(TERT-BUTYLSULFANYL)BENZENECARBALDEHYDE is employed as a versatile building block in organic chemistry for its capacity to participate in numerous chemical reactions, leading to the formation of a diverse array of organic compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 88357-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,5 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88357-16:
(7*8)+(6*8)+(5*3)+(4*5)+(3*7)+(2*1)+(1*6)=168
168 % 10 = 8
So 88357-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14OS/c1-11(2,3)13-10-6-4-9(8-12)5-7-10/h4-8H,1-3H3

88357-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butylsulfanylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-tert-Thiobutoxy-benzaldehyd

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:88357-16-8 SDS

88357-16-8Relevant academic research and scientific papers

COMPOUNDS AND METHOD OF USE

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Paragraph 1038, (2019/09/06)

This present disclosure relates to compounds with ferroptosis inducing activity, a method of treating a subject with cancer with the compounds, and combination treatments with a second therapeutic agent.

Bismuth(III)-Promoted Acetylation of Thioethers into Thioacetates

Jevric, Martyn,Petersen, Anne Ugleholdt,Mans?, Mads,Madsen, Anders,Nielsen, Mogens Br?ndsted

, p. 4675 - 4688 (2015/08/03)

The thioacetate group is extensively employed as an anchoring group for attachment of molecules onto gold surfaces or between electrodes in molecular electronics. On account of its ready hydrolysis, it is often incorporated in the last step of a synthetic

Copper-free sonogashira coupling reaction using a trans-spanning 1,2-Bis(2-thienylethynyl)benzene ligand

Atobe, Shingo,Sonoda, Motohiro,Suzuki, Yuki,Shinohara, Hiroyuki,Yamamoto, Takuya,Ogawa, Akiya

supporting information; experimental part, p. 980 - 982 (2012/02/01)

Novel copper-free Sonogashira coupling reaction of aryl halides with terminal acetylenes proceeded in the presence of 1,2-bis(2-thienylethynyl) benzene (1) as a trans-bidentatable ligand.

Novel cruciform structures as model compounds for coordination induced single molecule switches

Grunder, Sergio,Huber, Roman,Wu, Songmei,Schoenenberger, Christian,Calame, Michel,Mayor, Marcel

, p. 140 - 144 (2011/08/04)

We have synthesized various molecular cruciforms consisting of two different crossing π-systems and comprising crosswise arranged thiol- and pyridine-anchor groups. With these model compounds we strive towards the investigation of a new switching concept based on the potential dependent coordination of pyridines to gold electrodes in an electrochemical set-up. Integration of these cruciform molecules between both electrodes of a mechanically controlled break junction in a liquid environment gave insight into their single molecule transport properties. These studies allowed individual transport characteristics to be assigned to the bar subunits of the cruciforms but also revealed the remaining experimental challenges to realize the suggested switching concept. Schweizerische Chemische Gesellschaft.

Iron-catalyzed thioetherification of thiols with aryl iodides

Wu, Jhih-Ru,Lin, Che-Hung,Lee, Chin-Fa

supporting information; experimental part, p. 4450 - 4452 (2009/12/29)

FeCl3 in combination with bisphosphine ligands represents an efficient catalyst system for the cross-coupling of aryl- and alkyl thiols with aryl iodides, a broad spectrum of functional groups can be tolerated during the catalysis. The Royal Society of Chemistry 2009.

Synthesis and serotonin transporter activity of sulphur-substituted α-alkyl phenethylamines as a new class of anticancer agents

Cloonan, Suzanne M.,Keating, John J.,Butler, Stephen G.,Knox, Andrew J.S.,Jorgensen, Anne M.,Peters, Guenther H.,Rai, Dilip,Corrigan, Desmond,Lloyd, David G.,Williams, D. Clive,Meegan, Mary J.

scheme or table, p. 4862 - 4888 (2010/01/16)

The discovery that some serotonin reuptake transporter (SERT) ligands have the potential to act as pro-apoptotic agents in the treatment of cancer adds greatly to their diverse pharmacological application. 4-Methylthioamphetamine (MTA) is a selective ligand for SERT over other monoamine transporters. In this study, a novel library of structurally diverse 4-MTA analogues were synthesised with or without N-alkyl and/or C-α methyl or ethyl groups so that their potential SERT-dependent antiproliferative activity could be assessed. Many of the compounds displayed SERT-binding activity as well as cytotoxic activity. While there was no direct correlation between these two effects, a number of derivatives displayed anti-tumour effects in lymphoma, leukaemia and breast cancer cell lines, showing further potential to be developed as possible chemotherapeutic agents.

Palladium-catalyzed carbon-sulfur cross-coupling reactions with indium tri(organothiolate) and its application to sequential one-pot processes

Lee, Jae-Young,Phil, Ho Lee

supporting information; experimental part, p. 7413 - 7416 (2009/05/07)

(Chemical Equation Presented) It was found that indium tri(organothiolate) is an effective nucleophilic coupling partner in Pd-catalyzed C-S cross-coupling reactions to produce the functionalized sulfides in excellent yields with high atom efficiency and

Two-photon absorbing materials with quenched emission

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Page/Page column 6, (2009/01/20)

The present invention provides substituted phenanthroline compounds with high two photon absorption cross sections, as well as substituted phenanthroline compounds which additionally have quenched fluorescence emission upon two photon absorption.

New cruciform structures: Toward coordination induced single molecule switches

Grunder, Sergio,Huber, Roman,Horhoiu, Viviana,Gonzalez, Maria Teresa,Schoenenberger, Christian,Calame, Michel,Mayor, Marcel

, p. 8337 - 8344 (2008/03/11)

(Chemical Equation Presented) New cruciform structures 1-4 were synthesized to investigate a new single molecule switching mechanism arising from the interplay between the molecule and the electrode surface. These molecular cruxes consist of two rod-type

Fabrication of steady junctions consisting of α, ωbis(thioacetate) oligo(p-phenylene vinylene)s in nanogap electrodes

Liang, Tien-Tzu,Naitoh, Yasuhisa,Horikawa, Masayo,Ishida, Takao,Mizutani, Wataru

, p. 13720 - 13726 (2007/10/03)

For obtaining molecular devices using metal-molecule-metal junctions, it is necessary to fabricate a steady conductive bridge-structure; that is stable chemical bonds need to be established from a single conductive molecule to two facing electrodes. In th

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