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1207950-23-9

C24H24ClNO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207950-23-9 Structure

  • Basic information

    1. Product Name: C24H24ClNO3
    2. Synonyms: C24H24ClNO3
    3. CAS NO:1207950-23-9
    4. Molecular Formula:
    5. Molecular Weight: 409.912
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207950-23-9.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: C24H24ClNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H24ClNO3(1207950-23-9)
    11. EPA Substance Registry System: C24H24ClNO3(1207950-23-9)

  • 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: 1207950-23-9(Hazardous Substances Data)

1207950-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207950-23-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,9,5 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1207950-23:
(9*1)+(8*2)+(7*0)+(6*7)+(5*9)+(4*5)+(3*0)+(2*2)+(1*3)=139
139 % 10 = 9
So 1207950-23-9 is a valid CAS Registry Number.

1207950-23-9Downstream Products

1207950-23-9Relevant articles and documents

Chirality holds the key for potent inhibition of the botulinum neurotoxin serotype a protease

Stowe, G. Neil,Silhar, Peter,Hixon, Mark S.,Silvaggi, Nicholas R.,Allen, Karen N.,Moe, Scott T.,Jacobson, Alan R.,Barbieri, Joseph T.,Janda, Kim D.

, p. 756 - 759 (2010)

(Chemical Equetion Presentation) Botulinum neurotoxin serotype A (BoNT/A) is the most toxic protein known to man and also a bioterrorism agent. As defined by our previous research targeting the etiological agent responsible for BoNT/A intoxication, a protease, we now report on the asymmetric synthesis of four new BoNT/A inhibitors; the most potent of this series is roughly 2-fold more active than the best small molecule inhibitor currently known.

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