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CAS

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774580-81-3

3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 774580-81-3 Structure

  • Basic information

    1. Product Name: 3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate
    2. Synonyms: 3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate
    3. CAS NO:774580-81-3
    4. Molecular Formula:
    5. Molecular Weight: 562.662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 774580-81-3.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: 3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate(774580-81-3)
    11. EPA Substance Registry System: 3-(3-methoxy-4-(tosyloxy)phenyl)-2-((tosyloxy)methyl)propyl acetate(774580-81-3)

  • 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: 774580-81-3(Hazardous Substances Data)

774580-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774580-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,8 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 774580-81:
(8*7)+(7*7)+(6*4)+(5*5)+(4*8)+(3*0)+(2*8)+(1*1)=203
203 % 10 = 3
So 774580-81-3 is a valid CAS Registry Number.

774580-81-3Relevant articles and documents

Enantioselective synthesis of imperanene via enzymatic asymmetrization of an intermediary 1,3-diol

Carr, Jason A.,Bisht, Kirpal S.

, p. 3297 - 3300 (2007/10/03)

(Chemical Equation Presented) Using a chemoenzymatic synthetic strategy, (S)-imperanene and its (R)-enantiomer has been synthesized from vanillin in nine steps. The key step in the synthesis involves the use of Pseudomonas cepacia lipase (PS-30) to induce

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