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1036315-03-3

C19H13BrN2O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036315-03-3 Structure

  • Basic information

    1. Product Name: C19H13BrN2O2S
    2. Synonyms:
    3. CAS NO:1036315-03-3
    4. Molecular Formula:
    5. Molecular Weight: 413.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036315-03-3.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: C19H13BrN2O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H13BrN2O2S(1036315-03-3)
    11. EPA Substance Registry System: C19H13BrN2O2S(1036315-03-3)

  • 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: 1036315-03-3(Hazardous Substances Data)

1036315-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036315-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,3,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1036315-03:
(9*1)+(8*0)+(7*3)+(6*6)+(5*3)+(4*1)+(3*5)+(2*0)+(1*3)=103
103 % 10 = 3
So 1036315-03-3 is a valid CAS Registry Number.

1036315-03-3Downstream Products

1036315-03-3Relevant articles and documents

Synthesis and preliminary evaluation of some substituted coumarins as anticonvulsant agents

Amin, Kamelia M.,Rahman, Doaa E. Abdel,Al-Eryani, Yasmin A.

, p. 5377 - 5388 (2008)

Some new substituted coumarinylthiazolines, coumarinylthiazolidin-4-ones, and substituted chromenothiazoles were synthesized and evaluated for anticonvulsant activity. Some selected compounds were assayed against seizures induced by pentylenetetrazole (PTZ) and strychnine in mice. Compounds 3b, 6b, and 7b were the most active of the series against PTZ induced seizures. Compound 7b provided anticonvulsant activity (PD50 = 95 mg/kg, ip) at a dose 200 mg/kg compared to phenobarbital (PD50 = 16 mg/kg, ip) at a dose 30 mg/kg (90% protection). No clear correlation was observed between the antiepileptic activity and molecular lipophilicity descriptors of the tested compounds.

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