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1403959-05-6

C13H15N3O6S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403959-05-6 Structure

  • Basic information

    1. Product Name: C13H15N3O6S
    2. Synonyms: C13H15N3O6S
    3. CAS NO:1403959-05-6
    4. Molecular Formula:
    5. Molecular Weight: 341.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403959-05-6.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: C13H15N3O6S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H15N3O6S(1403959-05-6)
    11. EPA Substance Registry System: C13H15N3O6S(1403959-05-6)

  • 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: 1403959-05-6(Hazardous Substances Data)

1403959-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403959-05-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,9,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1403959-05:
(9*1)+(8*4)+(7*0)+(6*3)+(5*9)+(4*5)+(3*9)+(2*0)+(1*5)=156
156 % 10 = 6
So 1403959-05-6 is a valid CAS Registry Number.

1403959-05-6Downstream Products

1403959-05-6Relevant articles and documents

Organocatalyzed Baylis-Hillman reaction: An enantioselective approach

Thorat, Prashant B.,Goswami, Santosh V.,Khade, Bhimrao C.,Bhusare, Sudhakar R.

, p. 1320 - 1325 (2012/11/06)

A convenient protocol has been developed for the synthesis of Baylis-Hillman adducts in the presence of a base and an organocatalyst. We have designed and synthesized organocatalysts based on hydrogen bonding using a pyrrolidine ring as the backbone and applied them to Baylis-Hillman transformations. This method provides products in good to high yields (73-90%) and with excellent enantiomeric excesses (up to 96%) and reasonable reaction times.

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