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1023815-13-5

1-(4-fluorophenyl)-2-phenoxyethan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1023815-13-5 Structure

  • Basic information

    1. Product Name: 1-(4-fluorophenyl)-2-phenoxyethan-1-ol
    2. Synonyms: 1-(4-fluorophenyl)-2-phenoxyethan-1-ol
    3. CAS NO:1023815-13-5
    4. Molecular Formula:
    5. Molecular Weight: 232.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1023815-13-5.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-fluorophenyl)-2-phenoxyethan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-fluorophenyl)-2-phenoxyethan-1-ol(1023815-13-5)
    11. EPA Substance Registry System: 1-(4-fluorophenyl)-2-phenoxyethan-1-ol(1023815-13-5)

  • 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: 1023815-13-5(Hazardous Substances Data)

1023815-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1023815-13-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,8,1 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1023815-13:
(9*1)+(8*0)+(7*2)+(6*3)+(5*8)+(4*1)+(3*5)+(2*1)+(1*3)=105
105 % 10 = 5
So 1023815-13-5 is a valid CAS Registry Number.

1023815-13-5Relevant articles and documents

Exploring Tandem Ruthenium-Catalyzed Hydrogen Transfer and SNAr Chemistry

Polidano, Kurt,Reed-Berendt, Benjamin G.,Basset, Ana?s,Watson, Andrew J. A.,Williams, Jonathan M. J.,Morrill, Louis C.

supporting information, p. 6716 - 6719 (2017/12/26)

A hydrogen-transfer strategy for the catalytic functionalization of benzylic alcohols via electronic arene activation, accessing a diverse range of bespoke diaryl ethers and aryl amines in excellent isolated yields (38 examples, 70% average yield), is reported. Taking advantage of the hydrogen-transfer approach, the oxidation level of the functionalized products can be selected by judicious choice of simple and inexpensive additives.

Facile and selective hydrogenolysis of β-O-4 linkages in lignin catalyzed by Pd-Ni bimetallic nanoparticles supported on ZrO2

Zhang, Jia-Wei,Cai, Yao,Lu, Guo-Ping,Cai, Chun

supporting information, p. 6229 - 6235 (2016/12/03)

The β-O-4 linkage in lignin can be selectively cleaved by Pd-Ni bimetallic nanoparticles supported on ZrO2 using hydrogen gas as the hydrogen donor under ambient pressure and neutral conditions. Conspicuous enhancement in activity is observed compared with single nickel and palladium catalysts based on the results of experiments and characterization. Moreover, hydrogenation of the produced phenols is tuned by adjusting the amount of NaBH4. The catalyst can be reused over ten times in the model reaction and over five times in the hydrogenolysis of lignin without an obvious change in activity and selectivity.

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

supporting information; scheme or table, 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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