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5-Hexen-2-one, 4-methylene- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87061-19-6 Structure
  • Basic information

    1. Product Name: 5-Hexen-2-one, 4-methylene- (9CI)
    2. Synonyms: 5-Hexen-2-one, 4-methylene- (9CI)
    3. CAS NO:87061-19-6
    4. Molecular Formula: C7H10O
    5. Molecular Weight: 110.1537
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 87061-19-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Hexen-2-one, 4-methylene- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Hexen-2-one, 4-methylene- (9CI)(87061-19-6)
    11. EPA Substance Registry System: 5-Hexen-2-one, 4-methylene- (9CI)(87061-19-6)
  • 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: 87061-19-6(Hazardous Substances Data)

87061-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87061-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,6 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87061-19:
(7*8)+(6*7)+(5*0)+(4*6)+(3*1)+(2*1)+(1*9)=136
136 % 10 = 6
So 87061-19-6 is a valid CAS Registry Number.

87061-19-6Downstream Products

87061-19-6Relevant articles and documents

CONDENSATION DES NITRILES AVEC LES ORGANOZINCIQUES ALLYLIQUES. APPLICATIONS EN SERIE TERPENIQUE

Rousseau, G.,Drouin, J.

, p. 2307 - 2310 (2007/10/02)

The reaction of 3-bromomethyl-2,5-dihydrothiophen-1,1-dioxide 6 and 2-bromomethyl-1,3-butadiene 7 with nitriles in the presence of the zinc-silver couple leads to a mixture of ketones 8,9, the pyrolysis of which give the ketones 10 and 11, corresponding respectively to acylation of isoprene at its methyl group from 8, and at C-3 from 9.The reaction of bromide 7 with nitriles leads also to the formation of ketones 10 which by acid isomerisation give the ketones 12 corresponding to an acylation at C-1 of isoprene.In the same way the reaction of 2-(1'-methyl-4'-cyclohexenyl)-3-bromo propene 13 with 3,3-dimethyl acrylonitrile give β- atlantone 14 which is isomerised in acidic medium to α-atlantone 15. 10,11-dihydro α and β-atlantone 16, 17 are obtained by the same procedure from 13 and 3-methyl butyronitrile.

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