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CAS

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1402155-07-0

C17H23NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402155-07-0 Structure

  • Basic information

    1. Product Name: C17H23NO4
    2. Synonyms:
    3. CAS NO:1402155-07-0
    4. Molecular Formula:
    5. Molecular Weight: 305.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402155-07-0.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: C17H23NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H23NO4(1402155-07-0)
    11. EPA Substance Registry System: C17H23NO4(1402155-07-0)

  • 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: 1402155-07-0(Hazardous Substances Data)

1402155-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402155-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,1,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1402155-07:
(9*1)+(8*4)+(7*0)+(6*2)+(5*1)+(4*5)+(3*5)+(2*0)+(1*7)=100
100 % 10 = 0
So 1402155-07-0 is a valid CAS Registry Number.

1402155-07-0Downstream Products

1402155-07-0Relevant articles and documents

Double reductive amination and selective strecker reaction of a D-lyxaric aldehyde: Synthesis of diversely functionalized 3,4,5-trihydroxypiperidines

Matassini, Camilla,Mirabella, Stefania,Goti, Andrea,Cardona, Francesca

, p. 3920 - 3924 (2012/09/08)

A D-mannose-derived aldehyde with the D-lyxo configuration is a versatile key intermediate to functionally and stereochemically diversified piperidines. It allowed the synthesis of natural 3,4,5-trihydroxypiperidines and new analogs through a double reductive amination strategy and the synthesis of novel 2-cyanotrihydroxypiperidines through a highly regio-and diastereoselective Strecker reaction.

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