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1207985-10-1

C7H8O3S*C11H11NO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207985-10-1 Structure

  • Basic information

    1. Product Name: C7H8O3S*C11H11NO
    2. Synonyms:
    3. CAS NO:1207985-10-1
    4. Molecular Formula:
    5. Molecular Weight: 345.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207985-10-1.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: C7H8O3S*C11H11NO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C7H8O3S*C11H11NO(1207985-10-1)
    11. EPA Substance Registry System: C7H8O3S*C11H11NO(1207985-10-1)

  • 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: 1207985-10-1(Hazardous Substances Data)

1207985-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207985-10-1 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1207985-10:
(9*1)+(8*2)+(7*0)+(6*7)+(5*9)+(4*8)+(3*5)+(2*1)+(1*0)=161
161 % 10 = 1
So 1207985-10-1 is a valid CAS Registry Number.

1207985-10-1Downstream Products

1207985-10-1Relevant 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

, p. 684 - 687 (2010)

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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