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49651-35-6

2,6,6-trimethyl-5-morpholino-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 49651-35-6 Structure

  • Basic information

    1. Product Name: 2,6,6-trimethyl-5-morpholino-cyclohex-2-enone
    2. Synonyms:
    3. CAS NO:49651-35-6
    4. Molecular Formula:
    5. Molecular Weight: 223.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 49651-35-6.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: 2,6,6-trimethyl-5-morpholino-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6,6-trimethyl-5-morpholino-cyclohex-2-enone(49651-35-6)
    11. EPA Substance Registry System: 2,6,6-trimethyl-5-morpholino-cyclohex-2-enone(49651-35-6)

  • 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: 49651-35-6(Hazardous Substances Data)

49651-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49651-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49651-35:
(7*4)+(6*9)+(5*6)+(4*5)+(3*1)+(2*3)+(1*5)=146
146 % 10 = 6
So 49651-35-6 is a valid CAS Registry Number.

49651-35-6Downstream Products

49651-35-6Relevant articles and documents

Addition of Vinylketenes to Enamines. A Method for the Preparation of 6,6-Dialkylcyclohexa-2,4-dienones and 4,4-Dialkyl-2-vinylcyclobutenones

Berge, John M.,Rey, Max,Dreiding, Andre S.

, p. 2230 - 2241 (2007/10/02)

Drei Enamine (1-3) wurden mit fuenf Vinylketenen (5a-5e) (s.Schema 2) zur Reaktion gebracht.Die Vinylketene wurde in situ durch HCl-Eliminierung aus α,β-ungesaettigten Saeurechloriden mit Triaethylamin hergestellt.Die Cycloadditionen von 1-3 an 5a-5e fuehrten zu 6,6-Dialkyl-5-dialkylaminocycohex-2-enonen (kurz: Cyclohexenone) bzw. zu 3-Dialkylamino-4,4-dimethyl-2-vinylcyclobutanonen (kurz: Vinylcyclobutanone) oder zu einem Gemisch der beiden, je nach Natur der Partner bzw. des Loesungsmittels (s.Tab. 1).Durch oxidative Amin-Eliminierung wurden die Cyclohexenone in 6,6-Dialkylcyclohexa-2,4-dienone und die Vinylcyclobutanone in 4,4-Dialkyl-2-vinylcyclobutenone uebergefuehrt.Diese Reaktion stellt eine einfache Synthese von verschieden substituierten 6,6-Dialkylcyclohexa-2,4-dienonen bzw. 4,4-Dialkyl-2-vinylcyclobutenonen (siehe Schema 1) dar.

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