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Bis-(toluene-4-sulfonyl)-disulfane, also known as 4,4'-dithiodibenzenesulfonic acid or 4,4'-dithiodibenzenesulfonamide, is an organic compound with the chemical formula C14H14O4S4. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 180-190°C. bis-(toluene-4-sulfonyl)-disulfane is primarily used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds and as a protecting group in peptide synthesis. It is also employed in the production of dithiocarbamates, which are used as pesticides, rubber accelerators, and corrosion inhibitors. Due to its reactivity and potential applications, bis-(toluene-4-sulfonyl)-disulfane is an important intermediate in the chemical industry.

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  • 5962-57-2 Structure
  • Basic information

    1. Product Name: bis-(toluene-4-sulfonyl)-disulfane
    2. Synonyms: bis-(toluene-4-sulfonyl)-disulfane
    3. CAS NO:5962-57-2
    4. Molecular Formula:
    5. Molecular Weight: 374.527
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5962-57-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: bis-(toluene-4-sulfonyl)-disulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis-(toluene-4-sulfonyl)-disulfane(5962-57-2)
    11. EPA Substance Registry System: bis-(toluene-4-sulfonyl)-disulfane(5962-57-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5962-57-2(Hazardous Substances Data)

5962-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5962-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5962-57:
(6*5)+(5*9)+(4*6)+(3*2)+(2*5)+(1*7)=122
122 % 10 = 2
So 5962-57-2 is a valid CAS Registry Number.

5962-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-(toluene-4-sulfonyl)-disulfane

1.2 Other means of identification

Product number -
Other names Bis-(toluol-4-sulfonyl)-disulfan

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

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More Details:5962-57-2 SDS

5962-57-2Relevant articles and documents

Copper-Catalyzed C5-H Sulfenylation of Unprotected 8-Aminoquinolines Using Sulfonyl Hydrazides

Yu, Qing,Yang, Yiming,Wan, Jie-Ping,Liu, Yunyun

, p. 11385 - 11391 (2018/09/06)

The synthesis of C5-sulfenylated 8-aminoquinolines using unprotected 8-aminoquinolines and sulfonyl hydrazides is achieved via the catalysis of CuI. The reactions are hypothesized to proceed via the Cu(I)-Cu(II)-Cu(I) catalytic processes induced by aerobic oxidation and single-electron transfer on the Cu(II)-8-aminoquinoline complex. This work discloses an unprecedented step-efficient method for the synthesis of C5-sulfenylated 8-aminoquinolines bearing a useful free NH2 group.

Reactions of p-Toluenesulfinic Acid with Dialkoxy or Diamino Sulfides and Disulfides

Okawara, Tadashi,Yamasaki, Tetsuro,Sato, Kimitoshi,Miyazaki, Hiroyuki,Furukawa, Mitsuru

, p. 5225 - 5230 (2007/10/02)

The reactions of p-toluenesulfinic acid (1) with dialkoxy disulfides (2), dialkoxy sulfides (6), diamino disulfides (8), diamino sulfides (9), and diamino sulfoxides (15), were examined and found to give di-p-toluenesulfonyl disulfide (3), di-p-toluenesulfonyl sulfide (4), amino p-toluenesulfonyl disulfides (10), amino p-toluenesulfonyl sulfides (13), and p-toluenesulfinamides (16), respectively.Keywords - sulfinate S-nucleophile; intermolecular reaction; dialkoxy disulfide; dialkoxy sulfide; diamino disulfide; diamino sulfide; diamino sulfoxide; amino sulfonyl disulfide; amino sulfonyl sulfide

REACTIONS OF DIAMINO DISULFIDES, DIAMINO SULFIDES, AND DIAMINO SULFOXIDES WITH p-TOLUENESULFINIC ACID

Furukawa, Mitsuru,Sato, Kimitoshi,Okawara, Tadashi

, p. 2007 - 2010 (2007/10/02)

The reactions of diamino disulfides (2) and diamino sulfides (3) with p-toluenesulfinic acid (1) were found to give new types of compounds, amino p-toluenesulfonyl disulfides (5) and amino p-toluenesulfonyl sulfides (10), respectively.On the other hand, the reaction between dimorpholino sulfoxide (4) and 1 gave p-toluenesulfinylmorpholide (13).

Reactions of Toluene-p-sulphonic Thioanhydride with Sulphur Nucleophiles

Hansen, Holger C.,Senning, Alexander

, p. 692 - 693 (2007/10/02)

Ethoxythiocarbonyl p-tolylsulphonyl disulphide (5), benzylthio(thiocarbonyl) p-tolylsulphonyl disulphide (1c), and NN-dimethylthiocarbamoyl p-tolylsulphonyl disulphide (10) are formed in the reactions of toluene-p-sulphonic thioanhydride (3) with O-ethyl dithiocarbonate (4), benzyl trithiocarbonate (2), and NN-dimethyl dithiocarbamate (9) ions, respectively.

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