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CAS

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147092-04-4

Benzoic acid 2-phenylselanyl-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147092-04-4 Structure

  • Basic information

    1. Product Name: Benzoic acid 2-phenylselanyl-ethyl ester
    2. Synonyms: Benzoic acid 2-phenylselanyl-ethyl ester
    3. CAS NO:147092-04-4
    4. Molecular Formula:
    5. Molecular Weight: 305.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147092-04-4.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: Benzoic acid 2-phenylselanyl-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid 2-phenylselanyl-ethyl ester(147092-04-4)
    11. EPA Substance Registry System: Benzoic acid 2-phenylselanyl-ethyl ester(147092-04-4)

  • 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: 147092-04-4(Hazardous Substances Data)

147092-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147092-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,0,9 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147092-04:
(8*1)+(7*4)+(6*7)+(5*0)+(4*9)+(3*2)+(2*0)+(1*4)=124
124 % 10 = 4
So 147092-04-4 is a valid CAS Registry Number.

147092-04-4Downstream Products

147092-04-4Relevant articles and documents

A new methodology for the preparation of vinyl esters

Weinhouse,Janda

, p. 81 - 83 (2007/10/02)

A new methodology has been developed for the preparation of unsubstituted enol esters. Its application is demonstrated by the obtainment of vinyl aromatic α-amino esters. A brief investigation of the preparation of other hydrophobic vinyl esters proved successful. Because of the mild reaction conditions employed, it is believed this route should provide access to other enol esters.

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