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20126-56-1

Disulfide, 1-methylethyl phenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20126-56-1 Structure

  • Basic information

    1. Product Name: Disulfide, 1-methylethyl phenyl
    2. Synonyms:
    3. CAS NO:20126-56-1
    4. Molecular Formula: C9H12S2
    5. Molecular Weight: 184.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20126-56-1.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: Disulfide, 1-methylethyl phenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: Disulfide, 1-methylethyl phenyl(20126-56-1)
    11. EPA Substance Registry System: Disulfide, 1-methylethyl phenyl(20126-56-1)

  • 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: 20126-56-1(Hazardous Substances Data)

20126-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20126-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,2 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20126-56:
(7*2)+(6*0)+(5*1)+(4*2)+(3*6)+(2*5)+(1*6)=61
61 % 10 = 1
So 20126-56-1 is a valid CAS Registry Number.

20126-56-1Downstream Products

20126-56-1Relevant articles and documents

Substituted o-Aminophenols as Redox-Mediators in the Thiol Oxidation to Unsymmetrical Disulfides

Berberova, Nadezhda T.,Burmistrova, Daria A.,Galustyan, Andrey,Smolyaninov, Ivan V.

, (2021/06/17)

A number of substituted o-aminophenols has been investigated as redox mediators of the thiol oxidation to disulfides. The electrooxidation of o-aminophenols leads to the corresponding o-iminobenzoquinones. These compounds react with thiols in the solution with a formation of disulfides. It was established that the use of 4,6-di-tert-butyl-2-(tert-butylamino)phenol as a redox mediator can reduce the overpotential of the thiol oxidation by 0.2-1.4 V depending on the nature of the coupling thiols. The unsymmetrical disulfides with alkyl, aryl, and heteroaryl substituents were obtained as the result of the indirect electrosynthesis.

Sodium Tellurite as a Mild and Selective Oxidizing Agent for Thiols: Its Use in the One-Pot Synthesis of Unsymmetrical Disulfides

Suzuki, Hitomi,Kawato, Sei-ichi,Nasu, Akira

, p. 626 - 627 (2007/10/02)

Sodium tellurite acts as a mild and highly selective oxidizing agent for thiols under phase-transfer conditions at room temperature.Aromatic and benzylic thiols are rapidly converted to disulfides.Short-chain primary thiols undergo oxidation in preference to long-chain thiols.Secondary thiols are sluggish in oxidation and tertiary thiols remain intact.No overoxidation of the sulfur atom is observed.Similar results are also obtained with sodium tellurate.

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