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CAS

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1207985-07-6

C16H19NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207985-07-6 Structure

  • Basic information

    1. Product Name: C16H19NO3
    2. Synonyms: C16H19NO3
    3. CAS NO:1207985-07-6
    4. Molecular Formula:
    5. Molecular Weight: 273.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207985-07-6.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: C16H19NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H19NO3(1207985-07-6)
    11. EPA Substance Registry System: C16H19NO3(1207985-07-6)

  • 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: 1207985-07-6(Hazardous Substances Data)

1207985-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207985-07-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,9,8 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1207985-07:
(9*1)+(8*2)+(7*0)+(6*7)+(5*9)+(4*8)+(3*5)+(2*0)+(1*7)=166
166 % 10 = 6
So 1207985-07-6 is a valid CAS Registry Number.

1207985-07-6Downstream Products

1207985-07-6Relevant articles and documents

Chemoselectivity of the Ru-catalyzed cycloisomerization reaction for the synthesis of dihydropyrans; application to the synthesis of L-forosamine

Zacuto, Michael J.,Tomita, Daisuke,Pirzada, Zainab,Xu, Feng

supporting information; experimental part, p. 684 - 687 (2010/04/02)

Chemical Equation presented The chemoselectivity of a Ru-catalyzed cycloisomerization reaction has been established. The preference for O- capture of the vinylidene Intermediate allows for the synthesis of 4-aminodihydropyrans that are valuable synthetic Intermediates. The synthetic utility of these structures has been demonstrated in the synthesis of L-forosamine.

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