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CAS

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85842-10-0

C37H46N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85842-10-0 Structure

  • Basic information

    1. Product Name: C37H46N2O2
    2. Synonyms:
    3. CAS NO:85842-10-0
    4. Molecular Formula:
    5. Molecular Weight: 550.784
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85842-10-0.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: C37H46N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C37H46N2O2(85842-10-0)
    11. EPA Substance Registry System: C37H46N2O2(85842-10-0)

  • 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: 85842-10-0(Hazardous Substances Data)

85842-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85842-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,4 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85842-10:
(7*8)+(6*5)+(5*8)+(4*4)+(3*2)+(2*1)+(1*0)=150
150 % 10 = 0
So 85842-10-0 is a valid CAS Registry Number.

85842-10-0Downstream Products

85842-10-0Relevant articles and documents

Camoform analogs as potential agents against mefloquine resistant malaria

Hung,Werbel

, p. 61 - 66 (2007/10/02)

Analogs of 5,5'-di-2-propenyl-3,3'-bis(1-pyrrolidinylmethyl) [1,1'-biphenyl]-4,4'-diol 2 which exhibited modest activity against chloroquine- and mefloquine-resistant lines of Plasmodium berghei were prepared. Modifications of the Mannich side chain, the propenyl group, and analogs wherein a bridging atom was inserted between the phenyl rings were prepared. None of the structural changes provided an improvement in antimalarial activity over the lead compound in the P. berghei mouse system.

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