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CAS

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1414976-28-5

C16H23NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1414976-28-5 Structure

  • Basic information

    1. Product Name: C16H23NO2
    2. Synonyms: C16H23NO2
    3. CAS NO:1414976-28-5
    4. Molecular Formula:
    5. Molecular Weight: 261.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1414976-28-5.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: C16H23NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H23NO2(1414976-28-5)
    11. EPA Substance Registry System: C16H23NO2(1414976-28-5)

  • 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: 1414976-28-5(Hazardous Substances Data)

1414976-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414976-28-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,9,7 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1414976-28:
(9*1)+(8*4)+(7*1)+(6*4)+(5*9)+(4*7)+(3*6)+(2*2)+(1*8)=175
175 % 10 = 5
So 1414976-28-5 is a valid CAS Registry Number.

1414976-28-5Relevant articles and documents

PROCESS FOR PRODUCING ESTER COMPOUND

-

, (2014/04/17)

Compound (1) or a salt that is useful as an intermediate for the production of a medicine, an agrochemical or the like can be produced by a process including the following steps: (A) reacting an aldehyde (2) with nitromethane to produce a nitroaldehyde; (B) reacting the nitroaldehyde with an alcohol to produce a nitroacetal; (C) reducing the nitroacetal to produce an aminoacetal; (D) protecting an amino group in the aminoacetal to produce a protected aminoacetal; (E) treating the protected aminoacetal with an acid and subsequently with a base and then reacting the resultant product with a cyanating agent to produce a nitrile; (F) hydrolyzing the nitrile to produce a protected amino acid; and (G) substituting a group R5 in the protected amino acid by a hydrogen atom and protecting a carboxyl group therein.

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