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117516-70-8

1-tert-Butyl-3-(2,2-diethoxy-ethoxy)-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117516-70-8 Structure

  • Basic information

    1. Product Name: 1-tert-Butyl-3-(2,2-diethoxy-ethoxy)-benzene
    2. Synonyms:
    3. CAS NO:117516-70-8
    4. Molecular Formula:
    5. Molecular Weight: 266.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117516-70-8.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: 1-tert-Butyl-3-(2,2-diethoxy-ethoxy)-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-tert-Butyl-3-(2,2-diethoxy-ethoxy)-benzene(117516-70-8)
    11. EPA Substance Registry System: 1-tert-Butyl-3-(2,2-diethoxy-ethoxy)-benzene(117516-70-8)

  • 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: 117516-70-8(Hazardous Substances Data)

117516-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117516-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,1 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117516-70:
(8*1)+(7*1)+(6*7)+(5*5)+(4*1)+(3*6)+(2*7)+(1*0)=118
118 % 10 = 8
So 117516-70-8 is a valid CAS Registry Number.

117516-70-8Downstream Products

117516-70-8Relevant articles and documents

Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C-H arylation of 6,5-fused heterocycles

Saxena, Paridhi,Maida, Neha,Kapur, Manmohan

, p. 11187 - 11190 (2019)

A simple and effective Pd(ii)-catalyzed regioselective C(2)-H arylation of 6,5-fused heterocycles with dioxazolones as a masked ester surrogate under mild conditions is reported. The significance of the arylation is highlighted by the new reactivity demonstrated in dioxazolones via proximal C-H activation of the cyclic carbonate of the hydroxamic acid functionality under protic conditions.

PREPARATION AND CYCLIZATION OF ARYLOXYACETALDEHYDE ACETALS; A GENERAL SYNTHESIS OF 2,3-UNSUBSTITUTED BENZOFURANS

Barker, Peter,Finke, Paul,Thompson, Kevan

, p. 257 - 266 (2007/10/02)

A improved method for the preparation of 2,3-unsubstituted benzofurans is described.Specifically, the PPA catalysed cyclization of aryloxyacetaldehyde acetals to give (4-7)-substituted benzofurans has been achieved.

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