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80279-40-9

Disulfide, bis(2,4,6-trimethoxyphenyl) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80279-40-9 Structure

  • Basic information

    1. Product Name: Disulfide, bis(2,4,6-trimethoxyphenyl)
    2. Synonyms:
    3. CAS NO:80279-40-9
    4. Molecular Formula: C18H22O6S2
    5. Molecular Weight: 398.501
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80279-40-9.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, bis(2,4,6-trimethoxyphenyl)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Disulfide, bis(2,4,6-trimethoxyphenyl)(80279-40-9)
    11. EPA Substance Registry System: Disulfide, bis(2,4,6-trimethoxyphenyl)(80279-40-9)

  • 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: 80279-40-9(Hazardous Substances Data)

80279-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80279-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,7 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80279-40:
(7*8)+(6*0)+(5*2)+(4*7)+(3*9)+(2*4)+(1*0)=129
129 % 10 = 9
So 80279-40-9 is a valid CAS Registry Number.

80279-40-9Relevant articles and documents

Mass Spectral Behaviour of Some m-Dimethoxybenzene and sym-Trimethoxybenzene Sulphur Derivatives

Bottino, Francesco,Fradullo, Rosa,Pappalardo, Sebastino

, p. 289 - 293 (1981)

The mass spectra of fifteen m-dimethoxybenzene and sym-trimethoxybenzene sulphur derivatives (including thiols, sulphides, disulphides and trisulphides) have been investigated.Main fragmentation pathways have been proposed for each class of sulphur compou

Radical Ions, 81. ENDOR Spectroscopic Investigations of Radical Cations of Aromatic Organosulfur Compounds

Bock, H.,Hierholzer, B.,Rittmeyer, P.

, p. 187 - 204 (2007/10/02)

Conditions for ENDOR measurements of organosulfur radical cations are discussed and tested.The one electron oxidation of a variety of aromatic sulfur compounds comprising benzene-1,2-dithiole, 1,4-dithiine, thianthrene and diphenylsulfide derivatives as well as 33S isotope-marked bis(2,5-dimethoxyphenyl)disulfide is accomplished using the oxygen-free, powerful and selective AlCl3/H2CCl2 reagent.Partly with substantial structural changes, paramagnetic M.+ species of 1,2-benzodithiete, 1,4-dithiine, thianthrene and diphenyl sulfide result.Their temperature-dependent ENDOR signal patterns provide numerous information e.g. on radical cation structure and dynamics, on the rather high sulfur spin populations or on the spin rotation interaction dominated relaxation behaviour.Accordingly, to obtain optimum ENDOR effects in organosulfur radical cations low temperature measurements are required, and especially for still undiscovered 33S ENDOR couplings, small g factor anisotropies and 33S spin densities appear to be necessary. - Keywords: ENDOR (Special, General Triple) Spectra, Temperature Dependence, Organosulfur Radical Cations, Structural Changes, Molecular Dynamics

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