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1569090-26-1

C11H7ClN2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569090-26-1 Structure

  • Basic information

    1. Product Name: C11H7ClN2S
    2. Synonyms: C11H7ClN2S
    3. CAS NO:1569090-26-1
    4. Molecular Formula:
    5. Molecular Weight: 234.709
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569090-26-1.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: C11H7ClN2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H7ClN2S(1569090-26-1)
    11. EPA Substance Registry System: C11H7ClN2S(1569090-26-1)

  • 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: 1569090-26-1(Hazardous Substances Data)

1569090-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569090-26-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,0,9 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569090-26:
(9*1)+(8*5)+(7*6)+(6*9)+(5*0)+(4*9)+(3*0)+(2*2)+(1*6)=191
191 % 10 = 1
So 1569090-26-1 is a valid CAS Registry Number.

1569090-26-1Downstream Products

1569090-26-1Relevant articles and documents

Facile, efficient and eco-friendly synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles

Kuhn, Bruna L.,Fortes, Margiani P.,Kaufman, Teodoro S.,Silveira, Claudio C.

, p. 1648 - 1652 (2014)

A concise, two-step eco-friendly approach towards the synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles, is reported. The synthesis comprises the oxone-mediated thiocyanation of the starting heterocycles towards intermediate 3-thiocyanato indoles and 2-thiocyanato pyrroles, and their subsequent treatment with sodium azide in 2-propanol/water under zinc bromide promotion.

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