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9-benzyl-4-hydroxy-6-methoxy carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 247096-40-8 Structure
  • Basic information

    1. Product Name: 9-benzyl-4-hydroxy-6-methoxy carbazole
    2. Synonyms: 9-benzyl-4-hydroxy-6-methoxy carbazole
    3. CAS NO:247096-40-8
    4. Molecular Formula:
    5. Molecular Weight: 303.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247096-40-8.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: 9-benzyl-4-hydroxy-6-methoxy carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-benzyl-4-hydroxy-6-methoxy carbazole(247096-40-8)
    11. EPA Substance Registry System: 9-benzyl-4-hydroxy-6-methoxy carbazole(247096-40-8)
  • 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: 247096-40-8(Hazardous Substances Data)

247096-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247096-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,0,9 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 247096-40:
(8*2)+(7*4)+(6*7)+(5*0)+(4*9)+(3*6)+(2*4)+(1*0)=148
148 % 10 = 8
So 247096-40-8 is a valid CAS Registry Number.

247096-40-8Relevant articles and documents

AMINOALKOXY CARBAZOLES FOR THE TREATMENT OF CNS DISEASES

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, (2008/06/13)

The present invention provides aminoalkoxy carbazole derivatives, and more specifically, provides compounds of formula (I) wherein R 1, R 2, R 3, R 4, R 8 and R 9 are described herein. These compounds are 5-HT ligands, and are useful for treating diseases wherein modulation of 5-HT activity is desired.

Process for preparing 4-hdyroxy indole, indazole and carbazole compounds

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, (2008/06/13)

A process for preparing 4-hydroxy carbazoles useful as intermediates for preparing compounds that are useful for inhibiting sPLA2and novel intermediates.

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