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CAS

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164080-57-3

(Z)-1-(4-methoxyphenyl)-3-(2-methylprop-2-enylidene)-4-phenylazetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164080-57-3 Structure

  • Basic information

    1. Product Name: (Z)-1-(4-methoxyphenyl)-3-(2-methylprop-2-enylidene)-4-phenylazetidin-2-one
    2. Synonyms:
    3. CAS NO:164080-57-3
    4. Molecular Formula:
    5. Molecular Weight: 305.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164080-57-3.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: (Z)-1-(4-methoxyphenyl)-3-(2-methylprop-2-enylidene)-4-phenylazetidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-1-(4-methoxyphenyl)-3-(2-methylprop-2-enylidene)-4-phenylazetidin-2-one(164080-57-3)
    11. EPA Substance Registry System: (Z)-1-(4-methoxyphenyl)-3-(2-methylprop-2-enylidene)-4-phenylazetidin-2-one(164080-57-3)

  • 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: 164080-57-3(Hazardous Substances Data)

164080-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164080-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,0,8 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 164080-57:
(8*1)+(7*6)+(6*4)+(5*0)+(4*8)+(3*0)+(2*5)+(1*7)=123
123 % 10 = 3
So 164080-57-3 is a valid CAS Registry Number.

164080-57-3Upstream product

164080-57-3Downstream Products

164080-57-3Relevant articles and documents

3-(Prop-2-enylidene)azetidin-2-one derivatives: Synthesis, structure, and formation of 3-spiro-β-lactams via Diels-Alder reactions

Ruf,Otto

, p. 629 - 635 (1995)

Reactions of 3-silylated β-lactams (1) with α,β-unsaturated ketones give the propylidene-β-lactams 3 and the cycloalkenylidene derivatives 5. Structure and configuration are elucidated by spectroscopic methods, and the reactivity is discussed. While compounds 5 do not react with dienophiles, the (Z)-isomers of 3 are the favored substrates for Diels-Alder reactions yielding the spiro compounds 6 and 7.

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