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CAS

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1384440-07-6

1-(6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl)-2-methoxyethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384440-07-6 Structure

  • Basic information

    1. Product Name: 1-(6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl)-2-methoxyethanone
    2. Synonyms:
    3. CAS NO:1384440-07-6
    4. Molecular Formula:
    5. Molecular Weight: 393.913
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384440-07-6.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: 1-(6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl)-2-methoxyethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl)-2-methoxyethanone(1384440-07-6)
    11. EPA Substance Registry System: 1-(6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl)-2-methoxyethanone(1384440-07-6)

  • 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: 1384440-07-6(Hazardous Substances Data)

1384440-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384440-07-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,4,4 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384440-07:
(9*1)+(8*3)+(7*8)+(6*4)+(5*4)+(4*4)+(3*0)+(2*0)+(1*7)=156
156 % 10 = 6
So 1384440-07-6 is a valid CAS Registry Number.

1384440-07-6Downstream Products

1384440-07-6Relevant articles and documents

Synthesis and biological evaluation of licofelone derivatives as anticancer and anti-inflammatory agents

Liu, Wukun,Zhou, Jinpei,Zhang, Huibin,Qian, Hai,Yin, Jiahan,Bensdorf, Kerstin,Gust, Ronald

, p. 911 - 917 (2011)

Two C5-substituted licofelone derivatives were developed and investigated for cytotoxicity against mammary (MCF-7 and MDA-MB 231) as well as colon carcinoma (HT-29) cancer cells. Both compounds were at least 2-fold more active than 5-fluorouracil (5-FU) and licofelone against mammary carcinoma cells. At HT-29 cells, they were less active, but nevertheless distinctly as active as 5-FU and still 2-fold more active than licofelone. However, variation of the C5- carboxylic group results in an occasionally remarkable decrease of anti-inflammatory potency in in vitro and in vivo.

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