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28215-02-3

Disulfide, 2-nitrophenyl phenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28215-02-3 Structure

  • Basic information

    1. Product Name: Disulfide, 2-nitrophenyl phenyl
    2. Synonyms:
    3. CAS NO:28215-02-3
    4. Molecular Formula: C12H9NO2S2
    5. Molecular Weight: 263.341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28215-02-3.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, 2-nitrophenyl phenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: Disulfide, 2-nitrophenyl phenyl(28215-02-3)
    11. EPA Substance Registry System: Disulfide, 2-nitrophenyl phenyl(28215-02-3)

  • 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: 28215-02-3(Hazardous Substances Data)

28215-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28215-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,1 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28215-02:
(7*2)+(6*8)+(5*2)+(4*1)+(3*5)+(2*0)+(1*2)=93
93 % 10 = 3
So 28215-02-3 is a valid CAS Registry Number.

28215-02-3Relevant articles and documents

NFSI-catalyzed S[sbnd]S bond exchange reaction for the synthesis of unsymmetrical disulfides

Hu, Qingyue,Li, Zheng-Yi,Song, Mengjie,Sun, Xiaoqiang,Yang, Ke

supporting information, (2022/01/26)

The metal-free S[sbnd]S bond exchange reaction of symmetrical disulfides catalyzed by NFSI is described. This novel protocol provides a facile and efficient approach to accessing important unsymmetrical disulfides. Furthermore, this strategy could also be utilized in the late-stage functionalization of amino acids, drugs, and natural products. The broad substrate scope, good functional group tolerance and easy accessibility of catalyst indicate that this strategy affords a green and practical complementary method to various unsymmetrical disulfides.

Imination of sulfur-containing compounds: XXXV. New preparation method and oxidative benzenesulfonylimination of unsymmetrical disulfides

Koval'

, p. 232 - 234 (2007/10/03)

A new preparative method of synthesis was developed for unsymmetrical and symmetrical disulfides. This method involves sulfenylation of sodium thiolates with N-arenesulfenyl-N,N′-bis(arenesulfonyl)sulfinamidines. Imination of unsymmetrical disulfides with sodium chloroamides of sulfonic acids occurs at the more nucleophilic sulfur atom, affording N,N′ -bis(arenesulfonyl)sulfinamidines and symmetrical disulfides.

Ortho Effects in Organic Molecules on Electron Impact: 21 - Oxygen Transfers from the Ortho Nitro Group to Sulphur in N-Aryl-2-nitrobenzenesulphenamides and Phenyl-2-nitrophenyl Disulphide

Ramana, D. V.,Sundaram, N.,George, M.

, p. 926 - 930 (2007/10/02)

Fragment ions arising as a result of oxygen transfer from the nito group to sulphur have been noticed in N-aryl-2-nitrobenzenesulphenamides and phenyl-2-nitrophenyl disulphide.In the case of the former a double oxygen transfer to the sulphur has been noti

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