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1197285-84-9

C14H20NO3S(1+)*I(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1197285-84-9 Structure

  • Basic information

    1. Product Name: C14H20NO3S(1+)*I(1-)
    2. Synonyms: C14H20NO3S(1+)*I(1-)
    3. CAS NO:1197285-84-9
    4. Molecular Formula:
    5. Molecular Weight: 409.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1197285-84-9.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: C14H20NO3S(1+)*I(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H20NO3S(1+)*I(1-)(1197285-84-9)
    11. EPA Substance Registry System: C14H20NO3S(1+)*I(1-)(1197285-84-9)

  • 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: 1197285-84-9(Hazardous Substances Data)

1197285-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197285-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,2,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1197285-84:
(9*1)+(8*1)+(7*9)+(6*7)+(5*2)+(4*8)+(3*5)+(2*8)+(1*4)=199
199 % 10 = 9
So 1197285-84-9 is a valid CAS Registry Number.

1197285-84-9Relevant articles and documents

Efficient one-step synthesis of benzazoles in aqueous media

Boeini, Hassan Zali,Najafabadi, Khadijeh Hajibabaei

, p. 4926 - 4929 (2009)

Benzazoles (benzoxazoles, benzothiazoles, and benzimidazoles) were efficiently prepared by the aquatic reaction of the corresponding thioamidinium salts and 2-aminophenol, 2-aminothiophenol, and 1,2-diaminobenzene, respectively. The thioamidinium salt was successfully applied as an alternative to a carboxylic acid derivative to react smoothly with an amino precursor and in the presence of catalytic amounts of hexadecyltrimethylammonium bromide salt to produce benzazoles in good to excellent yields. Wiley-VCH Verlag GmbH & Co. KGaA 2009.

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