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1071569-05-5

C13H18O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1071569-05-5 Structure

  • Basic information

    1. Product Name: C13H18O3S
    2. Synonyms: C13H18O3S
    3. CAS NO:1071569-05-5
    4. Molecular Formula:
    5. Molecular Weight: 254.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1071569-05-5.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: C13H18O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H18O3S(1071569-05-5)
    11. EPA Substance Registry System: C13H18O3S(1071569-05-5)

  • 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: 1071569-05-5(Hazardous Substances Data)

1071569-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1071569-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,5,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1071569-05:
(9*1)+(8*0)+(7*7)+(6*1)+(5*5)+(4*6)+(3*9)+(2*0)+(1*5)=145
145 % 10 = 5
So 1071569-05-5 is a valid CAS Registry Number.

1071569-05-5Upstream product

1071569-05-5Downstream Products

1071569-05-5Relevant articles and documents

Asymmetric, organocatalytic, three-step synthesis of γ-hydroxy-(E)- α,β-unsaturated sulfones and esters

Petersen, Kimberly S.,Posner, Gary H.

supporting information; experimental part, p. 4685 - 4687 (2009/05/26)

(Chemical Equation Presented) Efficient and enantiocontrolled synthesis of γ-hydroxy-α,β-unsaturated sulfones and esters are reported through the reaction of enantioenriched a-selenyl aldehydes with EWG-stabilized carbanions and then a one-pot selenide ox

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