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1726-02-9

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1726-02-9 Usage

Description

Disulfide, bis(diphenylmethyl), also known as Dibenzhydryl Disulfide, is an organic compound with the molecular formula C28H22S2. It is a disulfide derivative of diphenylmethane and is characterized by its unique chemical structure, which consists of two phenyl rings connected through a methylene bridge and a disulfide bond. Disulfide, bis(diphenylmethyl) is known for its potential applications in various industries due to its chemical properties.

Uses

1. Pharmaceutical Industry:
Disulfide, bis(diphenylmethyl) is used as an impurity in the synthesis of Modafinil, a medication used to treat sleep disorders and improve wakefulness. Its presence in the synthesis process is crucial for the production of Modafinil, as it may affect the overall yield and quality of the final product.
2. Chemical Synthesis:
In the field of chemical synthesis, Disulfide, bis(diphenylmethyl) is used in reactions involving thioketones. Its unique disulfide bond allows for the formation of various complex organic compounds, which can be further utilized in the development of new materials and pharmaceuticals.
3. Research and Development:
Due to its unique chemical structure, Disulfide, bis(diphenylmethyl) is also used in research and development for the exploration of new chemical reactions and the synthesis of novel compounds. Its potential applications in various industries make it an interesting subject for further study and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1726-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1726-02:
(6*1)+(5*7)+(4*2)+(3*6)+(2*0)+(1*2)=69
69 % 10 = 9
So 1726-02-9 is a valid CAS Registry Number.

1726-02-9 Well-known Company Product Price

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  • (1445380)  Modafinil Related Compound E  United States Pharmacopeia (USP) Reference Standard

  • 1726-02-9

  • 1445380-20MG

  • 14,578.20CNY

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1726-02-9SDS

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 [(benzhydryldisulfanyl)-phenylmethyl]benzene

1.2 Other means of identification

Product number -
Other names DIS001

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:1726-02-9 SDS

1726-02-9Relevant articles and documents

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Minoura,Tsuboi

, p. 2064,2068 (1972)

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Imidazole Promoted Highly Efficient Large-Scale Thiol-Free Synthesis of Symmetrical Disulfides in Aqueous Media

Mokhtari, Babak,Kiasat, Ali Reza,Monjezi, Javid

, p. 1573 - 1579 (2015/09/15)

A highly efficient and environmentally friendly method for the imidazole promoted preparation of symmetrical organic disulfides from Bunte salts is described. This thiol-free procedure produces the desired disulfides even on a large scale by reaction of Bunte salts with imidazole in good to high yields in aqueous media.

A convenient synthesis of some symmetrical and unsymmetrical diarylmethyl sulfur and selenium compounds: X-ray crystal structure of diphenylmethylseleno-2-propene and bis[p-chlorophenyl(phenyl)methyl] diselenide

Bhasin,Singh, Neelam,Kumar, Rajeev,Gupta Deepali,Mehta,Klapoetke, Thomas M.,Crawford

, p. 3327 - 3334 (2007/10/03)

A number of novel and synthetically important symmetrical and unsymmetrical diarylmethyl sulfur and selenium compounds have been synthesized and characterized with the help of elemental analysis and various spectroscopic techniques. The methodology employ

PHASE TRANSFER CATALYZED DESULFURIZATION REACTIONS

Alper, Howard,Sibtain, Fazle,Heveling, Josef

, p. 5329 - 5332 (2007/10/02)

Mercaptans react with triiron dodecarbonyl or dicobalt octacarbonyl, under phase transfer catalysis conditions, to give hydrocarbons in good yields.

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