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145123-05-3

4-(1-Propyl-cyclohex-2-enyl)-morpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145123-05-3 Structure

  • Basic information

    1. Product Name: 4-(1-Propyl-cyclohex-2-enyl)-morpholine
    2. Synonyms:
    3. CAS NO:145123-05-3
    4. Molecular Formula:
    5. Molecular Weight: 209.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145123-05-3.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: 4-(1-Propyl-cyclohex-2-enyl)-morpholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(1-Propyl-cyclohex-2-enyl)-morpholine(145123-05-3)
    11. EPA Substance Registry System: 4-(1-Propyl-cyclohex-2-enyl)-morpholine(145123-05-3)

  • 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: 145123-05-3(Hazardous Substances Data)

145123-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145123-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,2 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145123-05:
(8*1)+(7*4)+(6*5)+(5*1)+(4*2)+(3*3)+(2*0)+(1*5)=93
93 % 10 = 3
So 145123-05-3 is a valid CAS Registry Number.

145123-05-3Downstream Products

145123-05-3Relevant articles and documents

3-Metallated enamines XI. Transmetallation of 3-Stannylated enamines - A new method to generate 1-aminoallyllithium compounds

Ahlbrecht,Weber

, p. 1018 - 1025 (2007/10/02)

The transmetallation of 3-stannylated enamines, 1-morpholino-3-(trialkylstannyl)cycloalk-1-enes and 3-morpholino-5-(tributylstannyl)hex-3-ene, with butyllithium is a new and general way to generate s1-aminoallyllithium compounds. Stabilization by aromatic substituents is not further necessarily as in the case of preparation by deprotonation and even the thermodynamically less stable exoamino derivatives are accessible. Therefore homoenolate-equivalents of cyclic ketones are made available. Thus, the corresponding 3-alkylated or 3-silylated cycloalkanones and alken-3-ones were prepared via the 1-morpholinoallyllithium compounds.

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