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78522-29-9

C34H24N2O2S6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78522-29-9 Structure

  • Basic information

    1. Product Name: C34H24N2O2S6
    2. Synonyms:
    3. CAS NO:78522-29-9
    4. Molecular Formula:
    5. Molecular Weight: 684.973
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78522-29-9.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: C34H24N2O2S6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C34H24N2O2S6(78522-29-9)
    11. EPA Substance Registry System: C34H24N2O2S6(78522-29-9)

  • 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: 78522-29-9(Hazardous Substances Data)

78522-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78522-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78522-29:
(7*7)+(6*8)+(5*5)+(4*2)+(3*2)+(2*2)+(1*9)=149
149 % 10 = 9
So 78522-29-9 is a valid CAS Registry Number.

78522-29-9Downstream Products

78522-29-9Relevant articles and documents

Studies on Heterocyclic Chemistry. Part 24. Syntheses of the 4-Arylisothiazol-3-yl O-Thioesters utilising the S-Thioester --> O-Thioester Rearrangements of the 4-Aryl-5-thioxo-3-isothiazolin-3-yl S-Thioesters induced by Acylation Reagents, Peracid, or N-B

Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Iori, Mistuo

, p. 1401 - 1406 (2007/10/02)

A number of 4-arylisothiazol-3-yl O-thioesters have been prepared utilising the S-thioester -> O-thioester rearrangements of the 4-aryl-5-thioxo-3-isothiazolin-3-yl S-thioesters (1).Reactions of the isothiazolines with acylation reagents (e.g. acyl chlori

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