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915127-49-0

1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 915127-49-0 Structure

  • Basic information

    1. Product Name: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide
    2. Synonyms:
    3. CAS NO:915127-49-0
    4. Molecular Formula: C13H9NO3SSe
    5. Molecular Weight: 338.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 915127-49-0.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: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(915127-49-0)
    11. EPA Substance Registry System: 1,2-Benzisothiazol-3(2H)-one, 2-(phenylseleno)-, 1,1-dioxide(915127-49-0)

  • 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: 915127-49-0(Hazardous Substances Data)

915127-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 915127-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,1,2 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 915127-49:
(8*9)+(7*1)+(6*5)+(5*1)+(4*2)+(3*7)+(2*4)+(1*9)=160
160 % 10 = 0
So 915127-49-0 is a valid CAS Registry Number.

915127-49-0Relevant articles and documents

N-Phenylselenosaccharin (NPSSac): a new electrophilic selenium-containing reagent

Tingoli, Marco,Diana, Rosita,Panunzi, Barbara

, p. 7529 - 7531 (2006)

A new reagent N-phenylselenosaccharin (NPSSac) was simply prepared and used as a source of the electrophilic phenylselenyl group. This relatively stable new compound was able to react with a series of electron rich organic molecules like alkenes in the pr

Synthesis method of selenium-containing isochroman compound

-

, (2021/05/29)

The invention discloses a synthesis method of a selenium-containing isochroman compound. The synthesis method comprises the following steps: under the protection of nitrogen, adding N-phenylseleno saccharin (NPSSac) into a reactor, then adding dichloromethane to completely dissolve the N-phenylseleno saccharin, adding a 1-[(cinnamoxy) methyl]-3, 4, 5-trimethoxy benzene compound and boron trifluoride diethyl etherate after the N-phenylseleno saccharin is completely dissolved, stirring at 20-60 DEG C for 2-6 hours until the reaction is complete, and after the reaction is finished, quenching, extracting, combining organic phases, drying, concentrating, separating and purifying to obtain the selenium-containing isochroman compound. The synthesis method disclosed by the invention is relatively easy to operate, mild in reaction condition, relatively high in yield, environment-friendly and suitable for large-scale industrial production.

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