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432038-16-9

6-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 432038-16-9 Structure

  • Basic information

    1. Product Name: 6-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran
    2. Synonyms: 6-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran
    3. CAS NO:432038-16-9
    4. Molecular Formula:
    5. Molecular Weight: 468.805
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 432038-16-9.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-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran(432038-16-9)
    11. EPA Substance Registry System: 6-benzenesulfinyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran(432038-16-9)

  • 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: 432038-16-9(Hazardous Substances Data)

432038-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 432038-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,0,3 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 432038-16:
(8*4)+(7*3)+(6*2)+(5*0)+(4*3)+(3*8)+(2*1)+(1*6)=109
109 % 10 = 9
So 432038-16-9 is a valid CAS Registry Number.

432038-16-9Upstream product

432038-16-9Relevant articles and documents

Synthesis of D-erythro-sphingosine and D-erythro-ceramide.

Milne, Jacqueline E,Jarowicki, Krzysztof,Kocienski, Philip J,Alonso, Jorge

, p. 426 - 427 (2002)

A 1,2-metallate rearrangment of a higher order cuprate derived from an alpha-lithiated xylal derivative and tridecyllithium is the key step in a synthesis of D-erythro-sphingosine and ceramide. A convenient method for preparing alpha-lithiated glycals from alpha-phenylsulfinyl glycals is also described.

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