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2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 946127-00-0 Structure
  • Basic information

    1. Product Name: 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran
    2. Synonyms: 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran
    3. CAS NO:946127-00-0
    4. Molecular Formula:
    5. Molecular Weight: 315.756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 946127-00-0.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: 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran(946127-00-0)
    11. EPA Substance Registry System: 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-7-hydroxy-1-benzopyran(946127-00-0)
  • 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: 946127-00-0(Hazardous Substances Data)

946127-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 946127-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,1,2 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 946127-00:
(8*9)+(7*4)+(6*6)+(5*1)+(4*2)+(3*7)+(2*0)+(1*0)=170
170 % 10 = 0
So 946127-00-0 is a valid CAS Registry Number.

946127-00-0Downstream Products

946127-00-0Relevant articles and documents

Discovery and structure-activity relationship of coumarin derivatives as TNF-α inhibitors

Cheng, Jie-Fei,Chen, Mi,Wallace, David,Tith, Sovouthy,Arrhenius, Thomas,Kashiwagi, Hirotaka,Ono, Yoshiyuki,Ishikawa, Akira,Sato, Haruhiko,Kozono, Toshiro,Sato, Hediki,Nadzan, Alex M.

, p. 2411 - 2415 (2004)

The discovery and structure-activity relationship of a novel series of coumarin-based TNF-α inhibitors is described. Starting from the initial lead 1a, various derivatives were prepared surrounding the coumarin core structure to optimize the in vitro inhibitory activity of TNF-α production by human peripheral blood mononuclear cells (hPBMC), stimulated by bacterial lipopolysaccharide (LPS). Selected compounds also demonstrated in vivo inhibition of TNF-α production in rats.

p27 PROTEIN INDUCER

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Paragraph 2941; 2955-2959, (2016/10/08)

The present invention provides a p27 protein inducing agent comprising a compound represented by general formula (11) below or pharmaceutically acceptable salt thereof as an active ingredient: wherein G 1 , G 2 , G 3 and G 8 are each independently selected from -N= etc., Ring G 6 is selected from divalent aryl etc., A is selected from amino etc., G 4 is selected from oxygen etc., G 5 is selected from oxygen etc., G 7 is selected from -CH 2 - etc., and R 2 is selected from C 1-6 alkyl etc.

p27 PROTEIN INDUCER

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, (2010/04/25)

The present invention provides a p27 protein inducing agent comprising a compound represented by general formula (11) below or pharmaceutically acceptable salt thereof as an active ingredient: wherein G1, G2, G3 and G8 are each independently selected from -N= etc., Ring G6 is selected from divalent aryl etc., A is selected from amino etc., G4 is selected from oxygen etc., G5 is selected from oxygen etc., G7 is selected from -CH2- etc., and R2 is selected from C1-6 alkyl etc.

NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY

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Page/Page column 201-202, (2008/12/04)

The present invention provides a compound represented by general formula (1) below or a pharmaceutically acceptable salt thereof: wherein: X is selected from heteroaryl etc., Y1 and Y2 are selected from -N= etc., Y3 and Y4 are selected from -CH= etc., A is selected from sulfamide etc., R1 is selected from hydrogen etc., and R2 is selected from C1-6 alkyl etc. The compound or salt has sufficiently high antitumor activity, and is useful in the treatment of cell proliferative disorders, particularly cancers. The present invention also provides a pharmaceutical composition containing the compound or salt as an active ingredient.

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