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1344112-05-5

(3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1344112-05-5 Structure

  • Basic information

    1. Product Name: (3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone
    2. Synonyms: (3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone
    3. CAS NO:1344112-05-5
    4. Molecular Formula:
    5. Molecular Weight: 304.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1344112-05-5.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: (3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone(1344112-05-5)
    11. EPA Substance Registry System: (3-hydroxy-4,5-dimethoxyphenyl)(3-hydroxy-4-methoxyphenyl)methanone(1344112-05-5)

  • 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: 1344112-05-5(Hazardous Substances Data)

1344112-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1344112-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,1,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1344112-05:
(9*1)+(8*3)+(7*4)+(6*4)+(5*1)+(4*1)+(3*2)+(2*0)+(1*5)=105
105 % 10 = 5
So 1344112-05-5 is a valid CAS Registry Number.

1344112-05-5Downstream Products

1344112-05-5Relevant articles and documents

Synthesis and biological evaluation of phenstatin metabolites

Ghinet, Alina,Rigo, Beno?t,Hénichart, Jean-Pierre,Le Broc-Ryckewaert, Delphine,Pommery, Jean,Pommery, Nicole,Thuru, Xavier,Quesnel, Bruno,Gautret, Philippe

, p. 6042 - 6054 (2011)

Previous investigations on the incubation of phenstatin with rat and human microsomal fractions revealed the formation of nine main metabolites. The structures of eight of these metabolites have been now confirmed by synthesis and their biological properties have been reported. Eaton's reagent was utilized as a convenient condensing agent, allowing, among others, a simple multigram scale preparation of phenstatin. Synthesized metabolites and related compounds were evaluated for their antiproliferative activity in the NCI-60 cancer cell line panel, and for their effect on microtubule assembly. Metabolite 23 (2′-methoxyphenstatin) exhibited the most potent in vitro cytotoxic activity: inhibition of the growth of K-562, NCI-H322M, NCI-H522, KM12, M14, MDA-MB-435, NCI/ADR-RES, and HS 578T cell lines with GI50 values 50 = 3.2 μM vs 15.0 μM) and induced G2/M arrest in murine leukemia DA1-3b cells. The identification of this active metabolite led to the design and synthesis of analogs with potent in vitro cytotoxicity and inhibition of microtubule assembly.

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