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CAS

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1393639-50-3

C15H14ClNO2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393639-50-3 Structure

  • Basic information

    1. Product Name: C15H14ClNO2S
    2. Synonyms:
    3. CAS NO:1393639-50-3
    4. Molecular Formula:
    5. Molecular Weight: 307.801
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393639-50-3.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: C15H14ClNO2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H14ClNO2S(1393639-50-3)
    11. EPA Substance Registry System: C15H14ClNO2S(1393639-50-3)

  • 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: 1393639-50-3(Hazardous Substances Data)

1393639-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393639-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,6,3 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1393639-50:
(9*1)+(8*3)+(7*9)+(6*3)+(5*6)+(4*3)+(3*9)+(2*5)+(1*0)=193
193 % 10 = 3
So 1393639-50-3 is a valid CAS Registry Number.

1393639-50-3Downstream Products

1393639-50-3Relevant articles and documents

Wake-promoting agents: Search for next generation modafinil: Part IV

Louvet, Philippe,Schweizer, Dominique,Gourdel, Marie-Edith,Riguet, Eric,Yue, Christoph,Marcy, Val R.,Lin, Yin Guo,Gruner, John,Lesur, Brigitte,Bacon, Edward R.,Chatterjee, Sankar

, p. 949 - 951 (2012/10/08)

In search of a next generation molecule to the novel wake promoting agent modafinil, a series of diphenyl ether derived wakefulness enhancing agents (in rat) was developed. From this work, racemic compound 16 was separated into its chiral enantiomers to p

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