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CAS

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1416427-50-3

C16H17NO5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1416427-50-3 Structure

  • Basic information

    1. Product Name: C16H17NO5
    2. Synonyms: C16H17NO5
    3. CAS NO:1416427-50-3
    4. Molecular Formula:
    5. Molecular Weight: 303.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1416427-50-3.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: C16H17NO5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H17NO5(1416427-50-3)
    11. EPA Substance Registry System: C16H17NO5(1416427-50-3)

  • 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: 1416427-50-3(Hazardous Substances Data)

1416427-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416427-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,4,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1416427-50:
(9*1)+(8*4)+(7*1)+(6*6)+(5*4)+(4*2)+(3*7)+(2*5)+(1*0)=143
143 % 10 = 3
So 1416427-50-3 is a valid CAS Registry Number.

1416427-50-3Downstream Products

1416427-50-3Relevant articles and documents

Enantioselective Michael addition of aldehydes to maleimides organocatalysed by chiral 1,2-diamines: An experimental and theoretical study

Avila, Angel,Chinchilla, Rafael,Gomez-Bengoa, Enrique,Najera, Carmen

, p. 1531 - 1535 (2013)

Simple and commercially available chiral 1,2-diamines were used as organocatalysts for the enantioselective conjugate addition of aldehydes, including α,α-disubstituted, to maleimides. The reaction was carried out in the presence of hexanedioic acid as an

Enantioselective Michael addition of α,α-disubstituted aldehydes to maleimides organocatalyzed by chiral primary amine-guanidines

Avila, Angel,Chinchilla, Rafael,Nájera, Carmen

, p. 1625 - 1627 (2013/02/22)

New primary amine-guanidines derived from the monoguanylation of (1S,2S)- and (1R,2R)-cyclohexane-1,2-diamine have been prepared and used as chiral organocatalysts for the enantioselective conjugate addition of α,α-disubstituted aldehydes to maleimides. T

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