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1191107-03-5

C22H24N2O5S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1191107-03-5 Structure

  • Basic information

    1. Product Name: C22H24N2O5S
    2. Synonyms: C22H24N2O5S
    3. CAS NO:1191107-03-5
    4. Molecular Formula:
    5. Molecular Weight: 428.509
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191107-03-5.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: C22H24N2O5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H24N2O5S(1191107-03-5)
    11. EPA Substance Registry System: C22H24N2O5S(1191107-03-5)

  • 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: 1191107-03-5(Hazardous Substances Data)

1191107-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191107-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,1,0 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1191107-03:
(9*1)+(8*1)+(7*9)+(6*1)+(5*1)+(4*0)+(3*7)+(2*0)+(1*3)=115
115 % 10 = 5
So 1191107-03-5 is a valid CAS Registry Number.

1191107-03-5Downstream Products

1191107-03-5Relevant articles and documents

Substituted Sulfonamide Compounds

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Page/Page column 46-47, (2009/10/30)

Substituted sulfonamide compounds corresponding to formula I: a process for their preparation, pharmaceutical compositions comprising such compounds, and the use of such substituted sulfonamide compounds in pharmaceutical compositions for the treatment of pain or other disorders or diseases that are mediated at least in part by B1R receptors.

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