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433223-59-7

C14H21N5O4S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 433223-59-7 Structure

  • Basic information

    1. Product Name: C14H21N5O4S2
    2. Synonyms:
    3. CAS NO:433223-59-7
    4. Molecular Formula:
    5. Molecular Weight: 387.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 433223-59-7.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: C14H21N5O4S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H21N5O4S2(433223-59-7)
    11. EPA Substance Registry System: C14H21N5O4S2(433223-59-7)

  • 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: 433223-59-7(Hazardous Substances Data)

433223-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 433223-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,2,2 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 433223-59:
(8*4)+(7*3)+(6*3)+(5*2)+(4*2)+(3*3)+(2*5)+(1*9)=117
117 % 10 = 7
So 433223-59-7 is a valid CAS Registry Number.

433223-59-7Relevant articles and documents

A novel and efficient regiospecific preparation of arenesulfonamide derivatives of 3,5-diamino-1,2,4-triazole

Chibale, Kelly,Dauvergne, Jér?me,Wyatt, Paul G.

, p. 185 - 190 (2007/10/03)

A new simple and efficient procedure was designed for the regiospecific preparation of arenesulfonamide derivatives of 3,5-diamino-1,2,4-triazole 1 which are precursors of N-([1,2,4] triazolo [1,5-a]pyrimidin-2-yl)arenesulfonamides 2, an important family of herbicidal and antibacterial agents. The key feature of this procedure is the preparation of a wide range of compounds 1 on a large scale, in pure form and high yield without the need for any workup or the use of the highly hazardous hydrazine. This was made possible by a novel tandem reaction promoted by sulfuryl chloride to effect the formation of the triazole ring.

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