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52923-38-3

(E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52923-38-3 Structure

  • Basic information

    1. Product Name: (E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide
    2. Synonyms: (E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide
    3. CAS NO:52923-38-3
    4. Molecular Formula:
    5. Molecular Weight: 281.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52923-38-3.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: (E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide(52923-38-3)
    11. EPA Substance Registry System: (E)-N-(4-(3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl)phenyl)acetamide(52923-38-3)

  • 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: 52923-38-3(Hazardous Substances Data)

52923-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52923-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52923-38:
(7*5)+(6*2)+(5*9)+(4*2)+(3*3)+(2*3)+(1*8)=123
123 % 10 = 3
So 52923-38-3 is a valid CAS Registry Number.

52923-38-3Downstream Products

52923-38-3Relevant articles and documents

Synthetic chalcones, flavanones, and flavones as antitumoral agents: Biological evaluation and structure-activity relationships

Cabrera, Mauricio,Simoens, Macarena,Falchi, Gabriela,Lavaggi, M. Laura,Piro, Oscar E.,Castellano, Eduardo E.,Vidal, Anabel,Azqueta, Amaia,Monge, Antonio,de Cerain, Adela Lopez,Sagrera, Gabriel,Seoane, Gustavo,Cerecetto, Hugo,Gonzalez, Mercedes

, p. 3356 - 3367 (2007)

A series of synthetic chalcones, flavanones, and flavones has been synthesized and evaluated for antitumor activity against the human kidney carcinoma cells TK-10, human mammary adenocarcinoma cells MCF-7 (estrogen receptor-positive), and human colon adenocarcinoma cells HT-29. The most active series is the chalcone ones with the best results against TK-10 and HT-29 cells. Fourteen out of 53 analyzed compounds resulted very active against at least two of the studied tumoral cells. Alkaline single cell gel electrophoresis, comet assay, was performed as a study of the chromosomal aberrations promoted by the compounds on normal cells. Four active and two inactive chalcones were studied in the comet assay against normal human kidney cells (HK-2). A structure-activity relationship analysis of these compounds was performed and for 4- and 3,4-disubstituted derivatives a quantitative correlation was obtained in the case of anti-HT-29 activity.

Skin Whitening Composition comprising Chalcone Derivatives

-

Paragraph 0195-0200, (2020/03/03)

The present invention relates to a skin whitening composition comprising a chalcone derivative. The composition can effectively suppress the production of melanin, and thus can be advantageously used for whitening of the skin in which melanin is excessive

Evaluation and optimization of the antimelanogenic activity of 1-(2-cyclohexylmethoxy-6-hydroxy-phenyl)-3-(4-hydroxymethyl-phenyl)-propenone derivatives

Kim, Byung-Hak,Hong, Soo-Nam,Ye, Sang-Kyu,Park, Jung-Youl

, (2019/04/17)

The chemical modification and optimization of biologically active compounds are essential steps in the identification of promising lead compounds for drug development. We previously reported the anti-melanogenic activity of 1-(2-cyclohexylmethoxy-6-hydrox

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