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200860-45-3

6-(3-Phenylsulfanyl-propyl)-1,4-dioxa-spiro[4.5]decane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 200860-45-3 Structure

  • Basic information

    1. Product Name: 6-(3-Phenylsulfanyl-propyl)-1,4-dioxa-spiro[4.5]decane
    2. Synonyms:
    3. CAS NO:200860-45-3
    4. Molecular Formula:
    5. Molecular Weight: 292.442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 200860-45-3.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: 6-(3-Phenylsulfanyl-propyl)-1,4-dioxa-spiro[4.5]decane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(3-Phenylsulfanyl-propyl)-1,4-dioxa-spiro[4.5]decane(200860-45-3)
    11. EPA Substance Registry System: 6-(3-Phenylsulfanyl-propyl)-1,4-dioxa-spiro[4.5]decane(200860-45-3)

  • 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: 200860-45-3(Hazardous Substances Data)

200860-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200860-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,8,6 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 200860-45:
(8*2)+(7*0)+(6*0)+(5*8)+(4*6)+(3*0)+(2*4)+(1*5)=93
93 % 10 = 3
So 200860-45-3 is a valid CAS Registry Number.

200860-45-3Relevant articles and documents

The preparation of synthetically useful carbonyl-protected δ- and ε-lithio ketones via reductive lithiation

Zhu, Shirong,Cohen, Theodore

, p. 17607 - 17624 (2007/10/03)

The aromatic radical-anion induced reductive lithiation of the acetals or thioacetals of δ- and ε-(phenylthio)ketones provides δ- and ε-lithioketone equivalents. Primary and tertiary organolithiums have been generated and the ketone function may be part o

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