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175434-86-3

C12H24OS is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 175434-86-3 Structure

  • Basic information

    1. Product Name: C12H24OS
    2. Synonyms: C12H24OS
    3. CAS NO:175434-86-3
    4. Molecular Formula:
    5. Molecular Weight: 216.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175434-86-3.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: C12H24OS(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H24OS(175434-86-3)
    11. EPA Substance Registry System: C12H24OS(175434-86-3)

  • 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: 175434-86-3(Hazardous Substances Data)

175434-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175434-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,3 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175434-86:
(8*1)+(7*7)+(6*5)+(5*4)+(4*3)+(3*4)+(2*8)+(1*6)=153
153 % 10 = 3
So 175434-86-3 is a valid CAS Registry Number.

175434-86-3Downstream Products

175434-86-3Relevant articles and documents

Erbium(III) triflate is a highly efficient catalyst for the synthesis of β-alkoxy alcohols, 1,2-diols and β-hydroxy sulfides by ring opening of epoxides

Dalpozzo, Renato,Nardi, Monica,Oliverio, Manuela,Paonessa, Rosina,Procopio, Antonio

, p. 3433 - 3438 (2009)

Chemo- and stereoselectivity in the ring-opening reaction of epoxides with erbium(III) triflate are described. Epoxides can be cleaved under neutral conditions with alcohols and thiols in the presence of catalytic amounts of Lewis acid, affording the corresponding β-alkoxy alcohols and β-hydroxy sulfides in high yields. In water, epoxide ring opening occurs to produce the corresponding diols in good yields.

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