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53063-64-2

Methyl-5-hydroxy-5-(2-methoxyphenyl)-3-oxopentanoat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53063-64-2 Structure

  • Basic information

    1. Product Name: Methyl-5-hydroxy-5-(2-methoxyphenyl)-3-oxopentanoat
    2. Synonyms:
    3. CAS NO:53063-64-2
    4. Molecular Formula:
    5. Molecular Weight: 252.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53063-64-2.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: Methyl-5-hydroxy-5-(2-methoxyphenyl)-3-oxopentanoat(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl-5-hydroxy-5-(2-methoxyphenyl)-3-oxopentanoat(53063-64-2)
    11. EPA Substance Registry System: Methyl-5-hydroxy-5-(2-methoxyphenyl)-3-oxopentanoat(53063-64-2)

  • 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: 53063-64-2(Hazardous Substances Data)

53063-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53063-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53063-64:
(7*5)+(6*3)+(5*0)+(4*6)+(3*3)+(2*6)+(1*4)=102
102 % 10 = 2
So 53063-64-2 is a valid CAS Registry Number.

53063-64-2Relevant articles and documents

Enantioselective vinylogous aldol reaction of Chan's diene catalyzed by hydrogen-bonding

Villano, Rosaria,Acocella, Maria Rosaria,Massa, Antonio,Palombi, Laura,Scettri, Arrigo

, p. 891 - 895 (2007)

Hydrogen-bonding activation of aromatic aldehydes by a TADDOL-derivative promotes the vinylogous aldol reaction of Chan's diene in moderate efficiency and enantioselectivity. Electron-poor aromatic aldehydes show an enhanced reactivity and a competing asy

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