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741292-53-5

(+)-(R)-1-(o-methoxyphenyl)-1-hydroxymethylphosphonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 741292-53-5 Structure

  • Basic information

    1. Product Name: (+)-(R)-1-(o-methoxyphenyl)-1-hydroxymethylphosphonic acid
    2. Synonyms:
    3. CAS NO:741292-53-5
    4. Molecular Formula:
    5. Molecular Weight: 218.146
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 741292-53-5.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: (+)-(R)-1-(o-methoxyphenyl)-1-hydroxymethylphosphonic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-(R)-1-(o-methoxyphenyl)-1-hydroxymethylphosphonic acid(741292-53-5)
    11. EPA Substance Registry System: (+)-(R)-1-(o-methoxyphenyl)-1-hydroxymethylphosphonic acid(741292-53-5)

  • 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: 741292-53-5(Hazardous Substances Data)

741292-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741292-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,2,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 741292-53:
(8*7)+(7*4)+(6*1)+(5*2)+(4*9)+(3*2)+(2*5)+(1*3)=155
155 % 10 = 5
So 741292-53-5 is a valid CAS Registry Number.

741292-53-5Downstream Products

741292-53-5Relevant articles and documents

Synthesis of optically active hydroxyphosphonates

Guliaiko, Irina,Nesterov, Vitaly,Sheiko, Sergei,Kolodiazhnyi, Oleg I.,Freytag, Matthias,Jones, Peter G.,Schmutzler, Reinhard

, p. 133 - 139 (2008)

The reduction of dimenthyl ketophosphonates with sodium borohydride involves asymmetric induction at the a-carbon atom, resulting in a small excess of the (R)-enantiomer of the a-hydroxyphosphonate formed. A higher ee purity was achieved if the reduction

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