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CAS

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1425667-67-9

C19H27NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1425667-67-9 Structure

  • Basic information

    1. Product Name: C19H27NO4
    2. Synonyms:
    3. CAS NO:1425667-67-9
    4. Molecular Formula:
    5. Molecular Weight: 333.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1425667-67-9.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: C19H27NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H27NO4(1425667-67-9)
    11. EPA Substance Registry System: C19H27NO4(1425667-67-9)

  • 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: 1425667-67-9(Hazardous Substances Data)

1425667-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1425667-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,5,6,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1425667-67:
(9*1)+(8*4)+(7*2)+(6*5)+(5*6)+(4*6)+(3*7)+(2*6)+(1*7)=179
179 % 10 = 9
So 1425667-67-9 is a valid CAS Registry Number.

1425667-67-9Downstream Products

1425667-67-9Relevant articles and documents

Access to 2,6-disubstituted piperidines: Control of the diastereoselectivity, scope, and limitations. applications to the stereoselective synthesis of (-)-solenopsine A and alkaloid (+)-241D

Abrunhosa-Thomas, Isabelle,Plas, Aurelie,Vogrig, Alexandre,Kandepedu, Nishanth,Chalard, Pierre,Troin, Yves

, p. 2511 - 2526 (2013/04/24)

Scope and limitations in the diastereoselective preparation of 2,6-cis or 2,6-trans disubstituted piperidines are described, through intramolecular reaction of chiral β′-carbamate-α,β-unsaturated ketone. This methodology has been applied to the total synthesis of a few well chosen examples, such as (-)-solenopsine A and alkaloid (+)-241D.

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