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CAS

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62086-75-3

(1RS,2SR)-1-(4'-chlorophenyl)-2-phenylethane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62086-75-3 Structure

  • Basic information

    1. Product Name: (1RS,2SR)-1-(4'-chlorophenyl)-2-phenylethane-1,2-diol
    2. Synonyms:
    3. CAS NO:62086-75-3
    4. Molecular Formula:
    5. Molecular Weight: 248.709
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62086-75-3.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: (1RS,2SR)-1-(4'-chlorophenyl)-2-phenylethane-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1RS,2SR)-1-(4'-chlorophenyl)-2-phenylethane-1,2-diol(62086-75-3)
    11. EPA Substance Registry System: (1RS,2SR)-1-(4'-chlorophenyl)-2-phenylethane-1,2-diol(62086-75-3)

  • 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: 62086-75-3(Hazardous Substances Data)

62086-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62086-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,8 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62086-75:
(7*6)+(6*2)+(5*0)+(4*8)+(3*6)+(2*7)+(1*5)=123
123 % 10 = 3
So 62086-75-3 is a valid CAS Registry Number.

62086-75-3Downstream Products

62086-75-3Relevant articles and documents

Studies on biotransformation of (±)-1-(4′-chlorophenyl)-2- phenylethanol

Bustillo, Antonio J.,Garcia-Pajon, Carlos M.,Aleu, Josefina,Hernandez-Galan, Rosario,Collado, Isidro G.

, p. 3755 - 3760 (2007/10/03)

The metabolism of (±)-1-(4′-chlorophenyl)-2-phenylethanol 1 by the phytopathogenic fungi Colletotrichum gloeosporioides and Botrytis cinerea has been studied. Regioselective monooxygenase-catalyzed hydroxylation of C-H bonds yielded the corresponding diols, the ratios of which showed a clear preference for the C-H benzylic bond. m-Hydroxylation in the substituted aromatic ring, a rarely described phenomenon, has been observed and with good enantioselectivity. The chemistry involved in determining the configuration of the biotransformation products is also described.

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