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119225-73-9

ethyl 2-cyclohex-1-enylprop-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119225-73-9 Structure

  • Basic information

    1. Product Name: ethyl 2-cyclohex-1-enylprop-2-enoate
    2. Synonyms: ethyl 2-cyclohex-1-enylprop-2-enoate
    3. CAS NO:119225-73-9
    4. Molecular Formula:
    5. Molecular Weight: 180.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119225-73-9.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: ethyl 2-cyclohex-1-enylprop-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-cyclohex-1-enylprop-2-enoate(119225-73-9)
    11. EPA Substance Registry System: ethyl 2-cyclohex-1-enylprop-2-enoate(119225-73-9)

  • 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: 119225-73-9(Hazardous Substances Data)

119225-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119225-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119225-73:
(8*1)+(7*1)+(6*9)+(5*2)+(4*2)+(3*5)+(2*7)+(1*3)=119
119 % 10 = 9
So 119225-73-9 is a valid CAS Registry Number.

119225-73-9Downstream Products

119225-73-9Relevant articles and documents

Catalytic Cleavage of C(sp2)-C(sp2) Bonds with Rh-Carbynoids

Wang, Zhaofeng,Jiang, Liyin,Sarró, Pau,Suero, Marcos G.

, p. 15509 - 15514 (2019)

We report a catalytic strategy that generates rhodium-carbynoids by selective diazo activation of designed carbyne sources. We found that rhodium-carbynoid species provoke C(sp2)-C(sp2) bond scission in alkenes by inserting a monovalent carbon unit between both sp2-hybridized carbons. This skeletal remodeling process accesses synthetically useful allyl cation intermediates that conduct to valuable allylic building blocks upon nucleophile attack. Our results rely on the formation of cyclopropyl-I(III) intermediates able to undergo electrocyclic ring-opening, following the Woodward-Hoffmann-DePuy rules.

REACTION DE CYCLOADDITION ENTRE L'ETHOXY-1 TRIMETHYSILYL-3 PROPYNE-1 ET LES CETONES α-HALOGENEES: SYNTHESE EN UNE ETAPE D'ESTERS DIENIQUES CONJUGUES

Pornet, J.,Rayadh, A.,Miginiac, L.

, p. 3065 - 3068 (1988)

In the presence of titanium tetrachloride, 1-ethoxy-3-trimethylsilyl-1-propyne easily reacts with many α-haloketones to lead to dienic conjugated esters; an α-ethylenic lactone may be obtained when the halogen is on a tertiary carbon atom.

Substituent effect on the chemical behaviour of some α-halogenated ketones and aldehydes with 1-ethoxy-3-trimethylsilylprop-1-yne

Zakarya, Driss,Rayadh, Ahmed,Samih, Mustapha,Lakhlifi, Tahar

, p. 2345 - 2348 (1994)

Principal Component Analysis (PCA) was carried out on the basis of property descriptions for a set of α-halogenated ketones and aldehydes. The obtained PCA model showed that the chemical behaviour of the compounds with 1-ethoxy-3-trimethylsilylprop-1-yne

A Novel and Stereodefined Synthesis of (E)-β-Ethoxycarbonylvinylsilanes: Regio- and Stereo-controlled Hydroethoxycarbonylation of Silylacetylenes by Palladium(II) Catalysis

Takeuchi, Ryo,Sugiura, Masaharu

, p. 1031 - 1038 (2007/10/02)

-SnCl2*2H2O catalysed hydroethoxycarbonylation of silylacetylenes 1 provided a novel and convenient synthesis of (E)-β-ethoxycarbonylvinylsilanes 2.The reactions, carried out under mild conditions (90 deg C, 20 kg cm-2) gave the pr

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