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CAS

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1363728-26-0

(E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1363728-26-0 Structure

  • Basic information

    1. Product Name: (E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate
    2. Synonyms: (E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate
    3. CAS NO:1363728-26-0
    4. Molecular Formula:
    5. Molecular Weight: 326.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1363728-26-0.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: (E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate(1363728-26-0)
    11. EPA Substance Registry System: (E)-1-(3-butyl-4-methyl-2-oxocyclopent-3-enylidene)-3-phenylpropyl acetate(1363728-26-0)

  • 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: 1363728-26-0(Hazardous Substances Data)

1363728-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363728-26-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,7,2 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1363728-26:
(9*1)+(8*3)+(7*6)+(6*3)+(5*7)+(4*2)+(3*8)+(2*2)+(1*6)=170
170 % 10 = 0
So 1363728-26-0 is a valid CAS Registry Number.

1363728-26-0Downstream Products

1363728-26-0Relevant articles and documents

Rhodium-catalyzed carbonylation of 3-acyloxy-1,4-enynes for the synthesis of cyclopentenones

Li, Xiaoxun,Huang, Suyu,Schienebeck, Casi M.,Shu, Dongxu,Tang, Weiping

, p. 1584 - 1587 (2012/05/07)

Functionalized cyclopentenones were synthesized by a Rh-catalyzed carbonylation of 3-acyloxy-1,4-enynes, derived from alkynes and α,β-unsaturated aldehydes. The reaction involved a Saucy-Marbet 1,3-acyloxy migration of propargyl esters and a [4 + 1] cycloaddition of the resulting acyloxy substituted vinylallene with CO.

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