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CAS

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1279715-01-3

C11H14O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1279715-01-3 Structure

  • Basic information

    1. Product Name: C11H14O3S
    2. Synonyms:
    3. CAS NO:1279715-01-3
    4. Molecular Formula:
    5. Molecular Weight: 226.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1279715-01-3.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: C11H14O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H14O3S(1279715-01-3)
    11. EPA Substance Registry System: C11H14O3S(1279715-01-3)

  • 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: 1279715-01-3(Hazardous Substances Data)

1279715-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1279715-01-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,7,1 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1279715-01:
(9*1)+(8*2)+(7*7)+(6*9)+(5*7)+(4*1)+(3*5)+(2*0)+(1*1)=183
183 % 10 = 3
So 1279715-01-3 is a valid CAS Registry Number.

1279715-01-3Downstream Products

1279715-01-3Relevant articles and documents

Catalytic asymmetric synthesis of γ-substituted vinyl sulfones

Lopez, Rosa,Zalacain, Maitane,Palomo, Claudio

, p. 2450 - 2457 (2011/05/02)

A fast new entry for the stereoselective construction of γ-substituted vinyl sulfones is presented. The key for success is the use of a readily available chiral secondary amine catalyst that allows the use of base-sensitive β-nitroethyl sulfones as masked β-sulfonyl vinyl anions in conjugate additions. The method performed in a three-step one-pot operation gives access to a great variety of vinyl sulfones in good yields and with excellent enantioselectivities. The method has also been extended to other relatively base-sensitive β-electron-withdrawing-substituted nitroalkanes to afford products with manifold functionality, providing a quick entry to very attractive synthetic intermediates for organic synthesis.

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