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114914-20-4

1-methyl-3-vinylmethylenecyclobutene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114914-20-4 Structure

  • Basic information

    1. Product Name: 1-methyl-3-vinylmethylenecyclobutene
    2. Synonyms: 1-methyl-3-vinylmethylenecyclobutene
    3. CAS NO:114914-20-4
    4. Molecular Formula:
    5. Molecular Weight: 94.1564
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114914-20-4.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: 1-methyl-3-vinylmethylenecyclobutene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-3-vinylmethylenecyclobutene(114914-20-4)
    11. EPA Substance Registry System: 1-methyl-3-vinylmethylenecyclobutene(114914-20-4)

  • 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: 114914-20-4(Hazardous Substances Data)

114914-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114914-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,1 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114914-20:
(8*1)+(7*1)+(6*4)+(5*9)+(4*1)+(3*4)+(2*2)+(1*0)=104
104 % 10 = 4
So 114914-20-4 is a valid CAS Registry Number.

114914-20-4Downstream Products

114914-20-4Relevant articles and documents

THE REDUCTION OF 2-VINYL-1,1-BIS(BROMOMETHYL)CYCLOPROPANE

Zefirov, N. S.,Kozhushkov, S. I.,Kuznetsova, T. S.,Sosonkin, I. M.,Domarev,A. M.,et al

, p. 1863 - 1873 (2007/10/02)

A study was carried out on the reduction of 2-vinyl-1,1-bis(bromomethyl)cyclopropane by various methods including electrochemical procedures.The major reaction pathways ential opening and expansion of the cyclopropane ring, while the product of the formation of a second three-membered ring, namely, vinylspiropentane, is formed in low yield.The probable radical mechanism for this reaction is discussed.

MECHANISM OF THE REACTION OF GLYCIDYL ESTERS WITH CARBOXYLIC ACIDS

Klebanov, M. S.,Kir'yazev, F. Yu.,Chervinskii, A. Yu.,Shologon, I. M.

, p. 2193 - 2196 (2007/10/02)

The kinetics of the reactions of 1-phenoxy-2,3-epoxypropane and 2,3-epoxypropylbenzoate with carboxylic acids were investigated.A new reaction mechanism is proposed to explain the anomalously high reactivity of the glycidyl esters.The mechanism involves protonation of the oxygen of the carbonyl group in the ester followed by intramolecular electrophilic attack on the oxirane oxygen by the carbonyl carbon atom, accompanied by opening of the epoxide ring and transfer of the acyl fragment in the glycidyl ester molecule.

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