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ethyl 2-(4-(tosyloxy)phenyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1361228-70-7 Structure
  • Basic information

    1. Product Name: ethyl 2-(4-(tosyloxy)phenyl)propanoate
    2. Synonyms: ethyl 2-(4-(tosyloxy)phenyl)propanoate
    3. CAS NO:1361228-70-7
    4. Molecular Formula:
    5. Molecular Weight: 348.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1361228-70-7.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: ethyl 2-(4-(tosyloxy)phenyl)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-(4-(tosyloxy)phenyl)propanoate(1361228-70-7)
    11. EPA Substance Registry System: ethyl 2-(4-(tosyloxy)phenyl)propanoate(1361228-70-7)
  • 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: 1361228-70-7(Hazardous Substances Data)

1361228-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361228-70-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,2,2 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1361228-70:
(9*1)+(8*3)+(7*6)+(6*1)+(5*2)+(4*2)+(3*8)+(2*7)+(1*0)=137
137 % 10 = 7
So 1361228-70-7 is a valid CAS Registry Number.

1361228-70-7Downstream Products

1361228-70-7Relevant articles and documents

Pd-catalyzed decarboxylative cross-couplings of potassium malonate monoesters with aryl halides

Feng, Yi-Si,Wu, Wei,Xu, Zhong-Qiu,Li, Yan,Li, Ming,Xu, Hua-Jian

, p. 2113 - 2120 (2012/03/26)

An efficient catalytic protocol for Pd-catalyzed decarboxylative cross-coupling of potassium malonate monoesters and derivatives with aryl bromides and chlorides are described. Because of its broad applicability, this new catalytic system provides an alternative method for the preparation of diverse aryl acetic acids and derivatives.

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