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1421348-08-4

C16H12F3NO2S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1421348-08-4 Structure

  • Basic information

    1. Product Name: C16H12F3NO2S2
    2. Synonyms: C16H12F3NO2S2
    3. CAS NO:1421348-08-4
    4. Molecular Formula:
    5. Molecular Weight: 371.404
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1421348-08-4.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: C16H12F3NO2S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H12F3NO2S2(1421348-08-4)
    11. EPA Substance Registry System: C16H12F3NO2S2(1421348-08-4)

  • 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: 1421348-08-4(Hazardous Substances Data)

1421348-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421348-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,3,4 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1421348-08:
(9*1)+(8*4)+(7*2)+(6*1)+(5*3)+(4*4)+(3*8)+(2*0)+(1*8)=124
124 % 10 = 4
So 1421348-08-4 is a valid CAS Registry Number.

1421348-08-4Upstream product

1421348-08-4Downstream Products

1421348-08-4Relevant articles and documents

New protein farnesyltransferase inhibitors in the 3-arylthiophene 2-carboxylic acid series: Diversification of the aryl moiety by solid-phase synthesis

Lethu, Sébastien,Bosc, Damien,Mouray, Elisabeth,Grellier, Philippe,Dubois, Jo?lle

, p. 163 - 171 (2013)

A new synthetic pathway was devised to reach tetrasubstituted 3-arylthiophene 2-carboxylic acids in a three-step solid-phase synthesis. This very efficient methodology provided more than 20 new compounds that were evaluated for their ability to inhibit protein farnesyltransferase from different species as well as Trypanosoma brucei and Plasmodium falciparum proliferation.

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