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748154-82-7

Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester

    Cas No: 748154-82-7

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  • 748154-82-7 Structure

  • Basic information

    1. Product Name: Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester
    2. Synonyms: Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester
    3. CAS NO:748154-82-7
    4. Molecular Formula:
    5. Molecular Weight: 369.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 748154-82-7.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: Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester(748154-82-7)
    11. EPA Substance Registry System: Bromo-acetic acid (1R,5S)-5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester(748154-82-7)

  • 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: 748154-82-7(Hazardous Substances Data)

748154-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 748154-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,8,1,5 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 748154-82:
(8*7)+(7*4)+(6*8)+(5*1)+(4*5)+(3*4)+(2*8)+(1*2)=187
187 % 10 = 7
So 748154-82-7 is a valid CAS Registry Number.

748154-82-7Relevant articles and documents

Enantioselective synthesis of phyllanthurinolactone, a leaf-closing substance of Phyllanthus urinaria L., and its analogs toward the development of molecular probes

Urakawa, Yoshifumi,Sugimoto, Takanori,Sato, Hirotaka,Ueda, Minoru

, p. 5885 - 5888 (2007/10/03)

We report enantioselective synthesis of phyllanthurinolactone (1), a leaf-closing substance of Phyllanthus urinaria L., and its analogs with sugars other than D-glucose. Structure-activity relationship study using them revealed that the structure of the sugar moiety did not affect their bioactivity at all. This result is very important for the development of molecular probes based on the structure of 1.

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