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132906-51-5

6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132906-51-5 Structure

  • Basic information

    1. Product Name: 6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one
    2. Synonyms: 6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one;6-Ethyl-2,3,4,9-tetrahydro-carbazol-1-one
    3. CAS NO:132906-51-5
    4. Molecular Formula: C14H15NO
    5. Molecular Weight: 213.275
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132906-51-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one(132906-51-5)
    11. EPA Substance Registry System: 6-ethyl-2,3,4,9-tetrahydro-1H-carbazol-1-one(132906-51-5)

  • 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: 132906-51-5(Hazardous Substances Data)

132906-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132906-51-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,0 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132906-51:
(8*1)+(7*3)+(6*2)+(5*9)+(4*0)+(3*6)+(2*5)+(1*1)=115
115 % 10 = 5
So 132906-51-5 is a valid CAS Registry Number.

132906-51-5Downstream Products

132906-51-5Relevant articles and documents

A novel necroptosis inhibitor - Necrostatin-21 and its SAR study

Wu, Zhijie,Li, Ying,Cai, Yu,Yuan, Junying,Yuan, Chengye

, p. 4903 - 4906 (2013/09/02)

An initial structure-activity relationship study of the novel necroptosis inhibitor Nec-21 was described. Any changes of the tetracyclic scaffold were detrimental for the activity. Introduction of a substituent to 7 or 8 position (e.g., cyano or methoxy group, respectively), would increase the activity. The 7 and 8-position disubstituted compound 17b was 35-fold as potent as the lead, while EC50 reached 14 nM.

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