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2-Hydroxy-4,5-bis-[2-(2-methoxy-ethoxy)-ethoxy]-benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 173313-07-0 Structure
  • Basic information

    1. Product Name: 2-Hydroxy-4,5-bis-[2-(2-methoxy-ethoxy)-ethoxy]-benzaldehyde
    2. Synonyms:
    3. CAS NO:173313-07-0
    4. Molecular Formula:
    5. Molecular Weight: 358.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173313-07-0.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-Hydroxy-4,5-bis-[2-(2-methoxy-ethoxy)-ethoxy]-benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxy-4,5-bis-[2-(2-methoxy-ethoxy)-ethoxy]-benzaldehyde(173313-07-0)
    11. EPA Substance Registry System: 2-Hydroxy-4,5-bis-[2-(2-methoxy-ethoxy)-ethoxy]-benzaldehyde(173313-07-0)
  • 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: 173313-07-0(Hazardous Substances Data)

173313-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173313-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,3,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 173313-07:
(8*1)+(7*7)+(6*3)+(5*3)+(4*1)+(3*3)+(2*0)+(1*7)=110
110 % 10 = 0
So 173313-07-0 is a valid CAS Registry Number.

173313-07-0Upstream product

173313-07-0Downstream Products

173313-07-0Relevant articles and documents

Synthesis and Evaluation of Novel Crowned Coumarins as Self-Catalytic Fluorescence Reagents

Takadate, Akira,Masuda, Toshinobu,Murata, Chiyomi,Tanaka, Toshiharu,Goya, Shujiro

, p. 3105 - 3110 (1995)

Three coumarin reagents carrying crown-ether moieties as catalytic sites for the fluorescence derivatization of carboxylic acids were designed and synthesized.The catalytic abilities of these reagents were evaluated based on the stability constants (Ks) for complexation with metal acetates in methanol.The derivatization reactions of carboxylic acids with these reagents proceeded self-catalytically without crown-ether catalysts, and gave the corresponding coumarin esters in good yields.It was found their reactivities significantly dependent upon the metal-binding ability of the reagent molecules from kinetic treatments of the reactions.The derivatized products showed remarkably high fluorescence quantum yields of above 0.8 in methanol.These results suggested that the functionalization of reagents was a quite useful approach for the development of new-type analytical reagents.

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