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3,4-Pentadienoic acid, 5-cyclohexyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54542-27-7 Structure
  • Basic information

    1. Product Name: 3,4-Pentadienoic acid, 5-cyclohexyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:54542-27-7
    4. Molecular Formula: C13H20O2
    5. Molecular Weight: 208.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54542-27-7.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: 3,4-Pentadienoic acid, 5-cyclohexyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-Pentadienoic acid, 5-cyclohexyl-, ethyl ester(54542-27-7)
    11. EPA Substance Registry System: 3,4-Pentadienoic acid, 5-cyclohexyl-, ethyl ester(54542-27-7)
  • 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: 54542-27-7(Hazardous Substances Data)

54542-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54542-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,4 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54542-27:
(7*5)+(6*4)+(5*5)+(4*4)+(3*2)+(2*2)+(1*7)=117
117 % 10 = 7
So 54542-27-7 is a valid CAS Registry Number.

54542-27-7Relevant articles and documents

Rhodium-Catalyzed Cyclization of Terminal and Internal Allenols: An Atom Economic and Highly Stereoselective Access Towards Tetrahydropyrans

Breit, Bernhard,Schmidt, Johannes P.

, p. 23485 - 23490 (2020/10/29)

A comprehensive study of a diastereoselective Rh-catalyzed cyclization of terminal and internal allenols is reported. The methodology allows the atom economic and highly syn-selective access to synthetically important 2,4-disubstituted and 2,4,6-trisubstituted tetrahydropyrans (THP). Furthermore, its utility and versatility are demonstrated by a great functional-group compatibility and the enantioselective total synthesis of (?)-centrolobine.

Ruthenium-catalyzed two-component addition to form 1,3-dienes: Optimization, scope, applications, and mechanism

Trost,Pinkerton,Seidel

, p. 12466 - 12476 (2007/10/03)

A two component coupling of an allene and an activated olefin to form 1,3-dienes has been developed. The requisite allenes are synthesized either from terminal alkynes by a one carbon homologation using copper(I) iodide, paraformaldehyde, and diisopropyla

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