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1176234-24-4

C13H17N5S*ClH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1176234-24-4 Structure

  • Basic information

    1. Product Name: C13H17N5S*ClH
    2. Synonyms:
    3. CAS NO:1176234-24-4
    4. Molecular Formula:
    5. Molecular Weight: 311.838
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1176234-24-4.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: C13H17N5S*ClH(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H17N5S*ClH(1176234-24-4)
    11. EPA Substance Registry System: C13H17N5S*ClH(1176234-24-4)

  • 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: 1176234-24-4(Hazardous Substances Data)

1176234-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1176234-24-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,6,2,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1176234-24:
(9*1)+(8*1)+(7*7)+(6*6)+(5*2)+(4*3)+(3*4)+(2*2)+(1*4)=144
144 % 10 = 4
So 1176234-24-4 is a valid CAS Registry Number.

1176234-24-4Upstream product

1176234-24-4Downstream Products

1176234-24-4Relevant articles and documents

Amide isosteres of oroidin: Assessment of antibiofilm activity and C. elegans toxicity

Richards, Justin J.,Reyes, Samuel,Stowe, Sean D.,Tucker, Ashley T.,Ballard, T. Eric,Mathies, Laura D.,Cavanagh, John,Melander, Christian

, p. 4582 - 4585 (2009)

The synthesis and antibiofilm activities of sulfonamide, urea, and thiourea oroidin analogues are described. The most active derivative was able to selectively inhibit P. aeruginosa biofilm development and is also shown to be nontoxic upward of 1 mM to th

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