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412274-38-5

1-(4-nitro-phenyl)-2-phenoxy-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 412274-38-5 Structure

  • Basic information

    1. Product Name: 1-(4-nitro-phenyl)-2-phenoxy-ethanol
    2. Synonyms:
    3. CAS NO:412274-38-5
    4. Molecular Formula:
    5. Molecular Weight: 259.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 412274-38-5.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: 1-(4-nitro-phenyl)-2-phenoxy-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-nitro-phenyl)-2-phenoxy-ethanol(412274-38-5)
    11. EPA Substance Registry System: 1-(4-nitro-phenyl)-2-phenoxy-ethanol(412274-38-5)

  • 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: 412274-38-5(Hazardous Substances Data)

412274-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 412274-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,2,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 412274-38:
(8*4)+(7*1)+(6*2)+(5*2)+(4*7)+(3*4)+(2*3)+(1*8)=115
115 % 10 = 5
So 412274-38-5 is a valid CAS Registry Number.

412274-38-5Relevant articles and documents

Chiral epoxides via borane reduction of 2-haloketones catalyzed by spiroborate ester: Application to the synthesis of optically pure 1,2-hydroxy ethers and 1,2-azido alcohols

Huang, Kun,Wang, Haiyang,Stepanenko, Viatcheslav,De Jesus, Melvin,Torruellas, Carilyn,Correa, Wildeliz,Ortiz-Marciales, Margarita

, p. 1883 - 1886 (2011/06/20)

An enantioselective borane-mediated reduction of a variety of 2-haloketones with 10% spiroaminoborate ester 1 as catalyst is described. By a simple basic workup of 2-halohydrins, optically active epoxides are obtained in high yield and with excellent enantiopurity (up to 99% ee). Ring-opening of oxiranes with phenoxides or sodium azide is investigated under different reaction conditions affording nonracemic 1,2-hydroxy ethers and 1,2-azido alcohols with excellent enantioselectivity (99% ee) and in good to high chemical yield. 2011 American Chemical Society.

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