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Benzo[b]thiophene, 2,3-dihydro-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26524-83-4 Structure
  • Basic information

    1. Product Name: Benzo[b]thiophene, 2,3-dihydro-, 1-oxide
    2. Synonyms:
    3. CAS NO:26524-83-4
    4. Molecular Formula: C8H8OS
    5. Molecular Weight: 152.217
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26524-83-4.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: Benzo[b]thiophene, 2,3-dihydro-, 1-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzo[b]thiophene, 2,3-dihydro-, 1-oxide(26524-83-4)
    11. EPA Substance Registry System: Benzo[b]thiophene, 2,3-dihydro-, 1-oxide(26524-83-4)
  • 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: 26524-83-4(Hazardous Substances Data)

26524-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26524-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26524-83:
(7*2)+(6*6)+(5*5)+(4*2)+(3*4)+(2*8)+(1*3)=114
114 % 10 = 4
So 26524-83-4 is a valid CAS Registry Number.

26524-83-4Relevant articles and documents

TiO2-sensitised photo-oxidation mechanism of indane and some of its hetero-analogues in deaerated CH3CN

Bettoni, Marta,Giacco, Tiziana Del,Rol, Cesare,Sebastiani, Giovanni V.

, p. 359 - 364 (2006)

A mechanistic study, principally based on product analysis, relative to the TiO2-photosensitized oxidation of indane and some of its hetero-analogues, in deaerated CH3CN and in the presence of Ag 2SO4, was performed. In particular: (i) 1-acetamidoindan (principal product), indene, 1-indanol and 1-indanone were obtained from indan; (ii) 5-methoxyindan gave 6-methoxyindene (principal product) and 5-methoxy-1-indanone; (iii) 2,3-dihydrobenzofuran, 2,3-dihydroindole and 2,3-dihydrobenzothiophene produced benzofuran, indole and benzothiophen (the last one accompanied by minor amounts of 2,3-dihydrobenzothiophene-1-oxide), respectively. Considering the previous studies on photo-oxidation of analogous substrates as benzylic derivatives (arenes, alcohols and ethers) and from reaction product profiles, an electron-transfer mechanism (from the substrate to the photogenerated hole) is suggested, where the radical cation intermediate should deprotonate to a benzylic radical. The carbocation obtained from the oxidation of this radical should competitively evolve to alkene, alcohol and acetamide. H218O labelling photo-oxidation experiments suggest that the ketone, when present, should derive from the substrate, through the alcohol as intermediate. Copyright

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