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CAS

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1446088-43-2

C17H28O4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446088-43-2 Structure

  • Basic information

    1. Product Name: C17H28O4S
    2. Synonyms:
    3. CAS NO:1446088-43-2
    4. Molecular Formula:
    5. Molecular Weight: 328.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446088-43-2.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: C17H28O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H28O4S(1446088-43-2)
    11. EPA Substance Registry System: C17H28O4S(1446088-43-2)

  • 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: 1446088-43-2(Hazardous Substances Data)

1446088-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446088-43-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,0,8 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1446088-43:
(9*1)+(8*4)+(7*4)+(6*6)+(5*0)+(4*8)+(3*8)+(2*4)+(1*3)=172
172 % 10 = 2
So 1446088-43-2 is a valid CAS Registry Number.

1446088-43-2Downstream Products

1446088-43-2Relevant articles and documents

Hydroalkoxylation of unactivated olefins with carbon radicals and carbocation species as key intermediates

Shigehisa, Hiroki,Aoki, Tatsuya,Yamaguchi, Sumiko,Shimizu, Nao,Hiroya, Kou

supporting information, p. 10306 - 10309 (2013/08/23)

A unique Markovnikov hydroalkoxylation of unactivated olefins with a cobalt complex, silane, and N-fluoropyridinium salt is reported. Further optimization of reaction conditions yielded high functional group tolerance and versatility of alcoholic solvent employed, including methanol, i-propanol, and t-butanol. Use of trifluorotoluene as a solvent made the use of alcohol in stoichiometric amount possible. Mechanistic insight into this novel catalytic system is also discussed. Experimental results suggest that catalysis involves both carbon radical and carbocation intermediates.

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