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1431570-06-7

C20H17NO5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1431570-06-7 Structure

  • Basic information

    1. Product Name: C20H17NO5
    2. Synonyms:
    3. CAS NO:1431570-06-7
    4. Molecular Formula:
    5. Molecular Weight: 351.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431570-06-7.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: C20H17NO5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H17NO5(1431570-06-7)
    11. EPA Substance Registry System: C20H17NO5(1431570-06-7)

  • 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: 1431570-06-7(Hazardous Substances Data)

1431570-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431570-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,5,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1431570-06:
(9*1)+(8*4)+(7*3)+(6*1)+(5*5)+(4*7)+(3*0)+(2*0)+(1*6)=127
127 % 10 = 7
So 1431570-06-7 is a valid CAS Registry Number.

1431570-06-7Downstream Products

1431570-06-7Relevant articles and documents

Synthetic approaches toward the marine alkaloid prenostodione

Badenock, Jeanese C.,Jordan, Jason A.,Gribble, Gordon W.

, p. 2759 - 2762 (2013/06/05)

An efficient synthesis of the core of prenostodione (3) is described herein featuring the base condensation of BOC-protected indole diesters 21 and 24 with p-methoxybenzaldehyde (22) and 4-[(t-butyldimethylsilyl)oxy]benzaldehyde (26). Attempts at selective saponification of the resultant diesters yielded isoprenostodione (3a) bearing the ester functionality at the C-3 position of the indole ring.

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