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2-Azetidinone, 3-methoxy-1-(4-methoxyphenyl)-4-[1-[(trimethylsilyl)oxy]ethenyl]-, (3S,4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 804563-07-3 Structure
  • Basic information

    1. Product Name: 2-Azetidinone, 3-methoxy-1-(4-methoxyphenyl)-4-[1-[(trimethylsilyl)oxy]ethenyl]-, (3S,4S)-
    2. Synonyms:
    3. CAS NO:804563-07-3
    4. Molecular Formula: C16H23NO4Si
    5. Molecular Weight: 321.448
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 804563-07-3.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: 2-Azetidinone, 3-methoxy-1-(4-methoxyphenyl)-4-[1-[(trimethylsilyl)oxy]ethenyl]-, (3S,4S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azetidinone, 3-methoxy-1-(4-methoxyphenyl)-4-[1-[(trimethylsilyl)oxy]ethenyl]-, (3S,4S)-(804563-07-3)
    11. EPA Substance Registry System: 2-Azetidinone, 3-methoxy-1-(4-methoxyphenyl)-4-[1-[(trimethylsilyl)oxy]ethenyl]-, (3S,4S)-(804563-07-3)
  • 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: 804563-07-3(Hazardous Substances Data)

804563-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 804563-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,5,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 804563-07:
(8*8)+(7*0)+(6*4)+(5*5)+(4*6)+(3*3)+(2*0)+(1*7)=153
153 % 10 = 3
So 804563-07-3 is a valid CAS Registry Number.

804563-07-3Upstream product

804563-07-3Relevant articles and documents

A cation-exchange resin promoted imino aldol reaction, leading to the synthesis of 2-isocephem and 2-oxa-isocephem

Shimizu, Makoto,Tachi, Masanori,Hachiya, Iwao

, p. 1394 - 1395 (2004)

Imino aldol reaction of ketene silyl acetals with the chiral imine 1 proceeds smoothly to give β-amino esters in good yields with high diasetereoselectivity under the influence of a cation-exchange resin, and the subsequent functional group transformation

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