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CAS

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1412896-01-5

C19H13Cl2N3O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1412896-01-5 Structure

  • Basic information

    1. Product Name: C19H13Cl2N3O2S
    2. Synonyms: C19H13Cl2N3O2S
    3. CAS NO:1412896-01-5
    4. Molecular Formula:
    5. Molecular Weight: 418.303
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1412896-01-5.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: C19H13Cl2N3O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H13Cl2N3O2S(1412896-01-5)
    11. EPA Substance Registry System: C19H13Cl2N3O2S(1412896-01-5)

  • 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: 1412896-01-5(Hazardous Substances Data)

1412896-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1412896-01-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,2,8,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1412896-01:
(9*1)+(8*4)+(7*1)+(6*2)+(5*8)+(4*9)+(3*6)+(2*0)+(1*1)=155
155 % 10 = 5
So 1412896-01-5 is a valid CAS Registry Number.

1412896-01-5Downstream Products

1412896-01-5Relevant articles and documents

Substituted pyrazolones require N2 hydrogen bond donating ability to protect against cytotoxicity from protein aggregation of mutant superoxide dismutase 1

Trippier, Paul C.,Benmohammed, Radhia,Kirsch, Donald R.,Silverman, Richard B.

supporting information, p. 6647 - 6650 (2013/01/14)

Amyotrophic lateral sclerosis (ALS) is a debilitating and fatal neurodegenerative disease. Although the cause remains unknown, misfolded protein aggregates are seen in neurons of sporadic ALS patients, and familial ALS mutations, including mutations in su

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