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ethyl 5-(cyclohexylamino)-5-oxopentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448862-11-0 Structure
  • Basic information

    1. Product Name: ethyl 5-(cyclohexylamino)-5-oxopentanoate
    2. Synonyms: ethyl 5-(cyclohexylamino)-5-oxopentanoate
    3. CAS NO:1448862-11-0
    4. Molecular Formula:
    5. Molecular Weight: 241.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448862-11-0.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 5-(cyclohexylamino)-5-oxopentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 5-(cyclohexylamino)-5-oxopentanoate(1448862-11-0)
    11. EPA Substance Registry System: ethyl 5-(cyclohexylamino)-5-oxopentanoate(1448862-11-0)
  • 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: 1448862-11-0(Hazardous Substances Data)

1448862-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448862-11-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,8,6 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1448862-11:
(9*1)+(8*4)+(7*4)+(6*8)+(5*8)+(4*6)+(3*2)+(2*1)+(1*1)=190
190 % 10 = 0
So 1448862-11-0 is a valid CAS Registry Number.

1448862-11-0Downstream Products

1448862-11-0Relevant articles and documents

Catalytic redox amidations of aldehydes with a polymer-supported peptide-N-heterocyclic carbene multifunctional catalyst

Gondo, Chenaimwoyo A.,Bode, Jeffrey W.

supporting information, p. 1205 - 1210 (2013/07/11)

We have prepared an oligomeric histidine-bound N-heterocyclic carbene precursor by coupling a carboxylic acid functionalized 1,2,4-triazolium salt to a peptide using solid-phase peptide synthesis. We have demonstrated that the resulting multifunctional resin-bound catalyst cooperatively facilitates redox amidation reactions of aldehydes and amines, a reaction not catalyzed by N-heterocyclic carbenes alone. Georg Thieme Verlag Stuttgart New York.

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