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Cyclohexanone, 4-(butylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 192373-10-7 Structure
  • Basic information

    1. Product Name: Cyclohexanone, 4-(butylamino)-
    2. Synonyms:
    3. CAS NO:192373-10-7
    4. Molecular Formula: C10H19NO
    5. Molecular Weight: 169.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 192373-10-7.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: Cyclohexanone, 4-(butylamino)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanone, 4-(butylamino)-(192373-10-7)
    11. EPA Substance Registry System: Cyclohexanone, 4-(butylamino)-(192373-10-7)
  • 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: 192373-10-7(Hazardous Substances Data)

192373-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192373-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,3,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 192373-10:
(8*1)+(7*9)+(6*2)+(5*3)+(4*7)+(3*3)+(2*1)+(1*0)=137
137 % 10 = 7
So 192373-10-7 is a valid CAS Registry Number.

192373-10-7Relevant articles and documents

Synthesis of a series of polar, orthogonally protected, α,α-disubstituted amino acids

Yokum, T. Scott,Bursavich, Matthew G.,Piha-Paul, Sarina A.,Hall, David A.,McLaughlin, Mark L.

, p. 4013 - 4016 (1997)

The synthesis of four novel, 'cationic', α,α-disubstituted amino acids is described. The new amino acids use an orthogonal protection scheme making them suitable for incorporation via solid-phase peptide synthesis.

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