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(5R)-5-chloro-5-phenyl-8,9,10,11-tetrahydro-4H-pyrido[3,2,1-jk]carbazole-4,6(5H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 300665-11-6 Structure
  • Basic information

    1. Product Name: (5R)-5-chloro-5-phenyl-8,9,10,11-tetrahydro-4H-pyrido[3,2,1-jk]carbazole-4,6(5H)-dione
    2. Synonyms:
    3. CAS NO:300665-11-6
    4. Molecular Formula: C21H12ClNO2
    5. Molecular Weight: 349.8102
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 300665-11-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 536.9°C at 760 mmHg
    3. Flash Point: 278.5°C
    4. Appearance: N/A
    5. Density: 1.41g/cm3
    6. Vapor Pressure: 1.34E-11mmHg at 25°C
    7. Refractive Index: 1.714
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (5R)-5-chloro-5-phenyl-8,9,10,11-tetrahydro-4H-pyrido[3,2,1-jk]carbazole-4,6(5H)-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5R)-5-chloro-5-phenyl-8,9,10,11-tetrahydro-4H-pyrido[3,2,1-jk]carbazole-4,6(5H)-dione(300665-11-6)
    12. EPA Substance Registry System: (5R)-5-chloro-5-phenyl-8,9,10,11-tetrahydro-4H-pyrido[3,2,1-jk]carbazole-4,6(5H)-dione(300665-11-6)
  • 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: 300665-11-6(Hazardous Substances Data)

300665-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300665-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,6,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 300665-11:
(8*3)+(7*0)+(6*0)+(5*6)+(4*6)+(3*5)+(2*1)+(1*1)=96
96 % 10 = 6
So 300665-11-6 is a valid CAS Registry Number.

300665-11-6Relevant articles and documents

Synthesis and reactions of pyrido[3,2,1-jk]carbazole-4,6-diones

Stadlbauer, Wolfgang,Van Dang, Hoai,Knobloch, Bernd

, p. 1039 - 1049 (2011/11/06)

Pyrido[3,2,1-jk]carbazoles 1, synthesized from carbazoles and alkyl- or arylmalonates, gave regioselective electrophilic substitution reactions at position 5 such as chlorination to 5-chloro derivatives 2, nitration to 5-nitro compounds 3, or hydroxylatio

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