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56135-07-0

1,1,1-Trifluor-2-hydroxy-2-ethoxy-2-phenylethan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56135-07-0 Structure

  • Basic information

    1. Product Name: 1,1,1-Trifluor-2-hydroxy-2-ethoxy-2-phenylethan
    2. Synonyms:
    3. CAS NO:56135-07-0
    4. Molecular Formula:
    5. Molecular Weight: 220.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56135-07-0.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: 1,1,1-Trifluor-2-hydroxy-2-ethoxy-2-phenylethan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,1-Trifluor-2-hydroxy-2-ethoxy-2-phenylethan(56135-07-0)
    11. EPA Substance Registry System: 1,1,1-Trifluor-2-hydroxy-2-ethoxy-2-phenylethan(56135-07-0)

  • 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: 56135-07-0(Hazardous Substances Data)

56135-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56135-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56135-07:
(7*5)+(6*6)+(5*1)+(4*3)+(3*5)+(2*0)+(1*7)=110
110 % 10 = 0
So 56135-07-0 is a valid CAS Registry Number.

56135-07-0Relevant articles and documents

Convenient stereoselective synthesis of β-perfluoroalkyl α,β-unsaturated esters via H?rner-Wadsworth-Emmons reactions

Yamazaki, Takashi,Mano, Noriko,Hikage, Reo,Kaneko, Tsutomu,Kawasaki-Takasuka, Tomoko,Yamada, Shigeyuki

, p. 8059 - 8066 (2015)

Condensation of H?rner-Wadsworth-Emmons reagents 3 and ketones 2 with a perfluoroalkyl (Rf) moiety prepared in situ was proved to be significantly efficient and powerful methods for the construction of a wide variety of α,β-unsaturated esters with Rf and R1 groups both at the β-position due to convenient avoidance of usually tedious as well as troublesome isolation steps of these ketones 2.

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