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1-(4-chlorophenyl)-2-[2-(4-chlorophenyl)-2-oxo-ethyl]disulfanyl-ethanone is a complex organic compound characterized by its unique molecular structure. It consists of a central ethane molecule with a disulfanyl group (S-S) attached to the second carbon. The first carbon is bonded to a 4-chlorophenyl group, while the second carbon is connected to a 2-oxo-ethyl group, which in turn is attached to another 4-chlorophenyl group. 1-(4-chlorophenyl)-2-[2-(4-chlorophenyl)-2-oxo-ethyl]disulfanyl-ethanone is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of certain drugs and agrochemicals. Its chemical properties, such as reactivity and stability, are influenced by the presence of the chlorine atoms and the disulfide bond, making it an interesting subject for further research and development.

5409-94-9

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5409-94-9 Usage

Chemical structure

1-(4-chlorophenyl)-2-[2-(4-chlorophenyl)-2-oxo-ethyl]disulfanyl-ethanone is a complex chemical compound with two phenyl rings and a disulfide bond.

Molar mass

367.29 g/mol

Structural features

The presence of disulfide bonds, which are known to play important roles in biological processes.

Potential applications

Likely has potential applications in the field of medicinal chemistry due to its structural features.

Further research

More research is needed to fully elucidate the properties and potential uses of 1-(4-chlorophenyl)-2-[2-(4-chlorophenyl)-2-oxo-ethyl]disulfanyl-ethanone.

Biological activity

Disulfide bonds are often incorporated into drug molecules to enhance their biological activity.

Chlorine atoms

Contains two chlorine atoms, which may contribute to its chemical reactivity and potential applications.

Carbonyl group

The presence of a carbonyl group (C=O) in the molecule, which is a common functional group in organic chemistry and can influence the compound's reactivity and properties.

Ethyl group

Contains an ethyl group (-CH2CH3), which may affect the compound's lipophilicity and solubility in different solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 5409-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5409-94:
(6*5)+(5*4)+(4*0)+(3*9)+(2*9)+(1*4)=99
99 % 10 = 9
So 5409-94-9 is a valid CAS Registry Number.

5409-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-2-[[2-(4-chlorophenyl)-2-oxoethyl]disulfanyl]ethanone

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:5409-94-9 SDS

5409-94-9Relevant academic research and scientific papers

An eight-membered N,N,S,S-heterocyclic compound: 4,7-bis(4-chlorophenyl)-3,8-di-hydro-1,2,5,6-dithiadiazocine

Rymarczyk, Beate M.,Preut, Hans,Kreher, Richard P.

, p. 931 - 933 (1997)

The eight-membered ring in the title compound, C16H12Cl2N2S2, adopts a non-planar conformation as expected, and the least-squares planes of the 4-substituted aromatic ring form a dihedral angle of 83.

Gas-Solid Chlorination of 4-Phenylthiazole-2(1H)-thione

Nalini, Veerapaneni,Desiraju, Gautam R.

, p. 1046 - 1048 (1987)

The title compound (1) is converted into an unusual chlorophenacyl disulphide (2) through a crystal structure controlled chlorination-oxidation reaction.

An efficient metal-free synthesis of organic disulfides from thiocyanates using poly-ionic resin hydroxide in aqueous medium

Sengupta, Debasish,Basu, Basudeb

supporting information, p. 2277 - 2281 (2013/05/08)

An efficient and metal-free method is described for the preparation of organic disulfides from alkyl and acyl methyl thiocyanates in the presence of poly-ionic resin hydroxide in aqueous medium. Further extension of this protocol has been tested using two different organyl thiocyanates to prepare unsymmetrical disulfides.

Synthesis of imidazolyl dithiocarbamates and their reactions with phenacyl bromides

El'Tsov,Mokrushin,Smirnova,Shafikov

experimental part, p. 882 - 888 (2012/02/05)

The reactions of ethyl (5-carbamoyl-3H-imidazol-4-yl)dithiocarbamate with phenacyl bromides afford the S-alkylation products as a mixture of E/Z-isomers, which undergo cyclization to 5-(2-oxo-4-arylthiazol-3-yl)-1H-imidazole-4- carboxamides under the acti

One-step synthesis of N-acetylcysteine and glutathione derivatives using the Ugi reaction

Zhdanko, Alexander G.,Gulevich, Anton V.,Nenajdenko, Valentine G.

experimental part, p. 4692 - 4702 (2009/10/02)

Fully protected natural and unnatural N-acetylcysteine, dipeptide Cys-Gly, glutathione, and homoglutathione derivatives were synthesized by the Ugi four-component reaction using various benzylthio aldehydes and ketones as carbonyl building blocks. The scope and limitations of the method were investigated. Formation of imidazoline by-products in the Ugi reaction was discussed. 2,2,2-Trifluoroethanol was shown to be a superior reaction media than methanol in some reactions. Also, the 4-methyl-2,6,7-trioxabicyclo[2.2.2]octyl derivative (OBO-ester) of isocyanoacetic acid was shown to be superior to use than ethyl isocyanoacetate as a peptide synthesis precursor in cases when higher reactivity of an isocyanide is required.

Mn(III)-based reactions of alkenes and alkynes with thiols. An approach toward substituted 2,3-dihydro-1,4-oxathiins and simple route to (E)-vinyl sulfides

Nguyen, Van-Ha,Nishino, Hiroshi,Kajikawa, Shougo,Kurosawa, Kazu

, p. 11445 - 11460 (2007/10/03)

The first example using manganese(III) acetate in the reaction of 1,1- diarylethenes with α-mercaptoketones was examined. A mixture of the ethenes and α-mercaptoketones was treated with manganese(III) acetate in acetic acid, affording cycloaddition products in moderate yields, together with substituted products. The reaction may involve the formation of a carbonation and subsequent cyclization to give the substituted 2,3-dihydro-1,4-oxathiin 3. A similar reaction with thioglycolic acid gave 1,4-oxathiolan-2-one 7. While thiyl radicals easily formed by manganese(III) oxidation with ethanethiol or benzenethiol reacted with alkynes to give preferentially (E)- vinyl sulfides 10 in quantitative yields.

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