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CAS

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211317-19-0

2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 211317-19-0 Structure

  • Basic information

    1. Product Name: 2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde
    2. Synonyms: 2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde
    3. CAS NO:211317-19-0
    4. Molecular Formula:
    5. Molecular Weight: 382.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 211317-19-0.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: 2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde(211317-19-0)
    11. EPA Substance Registry System: 2,2′-[ethane-1,2-diylbis(oxy)]di(5-tert-butyl)benzaldehyde(211317-19-0)

  • 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: 211317-19-0(Hazardous Substances Data)

211317-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211317-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,3,1 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 211317-19:
(8*2)+(7*1)+(6*1)+(5*3)+(4*1)+(3*7)+(2*1)+(1*9)=80
80 % 10 = 0
So 211317-19-0 is a valid CAS Registry Number.

211317-19-0Relevant articles and documents

Synthesis, structure, and extraction behavior of 4,5′,4″,5?-tetra-tert-butyltetrabenzo-24-crown-8

Levitskaia, Tatiana G.,Sachleben, Richard A.,Bryan, Jeffrey C.,Moyer, Bruce A.

, p. 808 - 814 (2001)

Isomerically pure 4,5′,4″,5?-tetra-tert-butyltetrabenzo-24-crown-8 was synthesized by a route that eliminates any need for isomer separation. Its structure was determined using single crystal X-ray diffraction methods. Since the observed saddle-shaped con

Mono- and diformylation of 4-substituted phenols: A new application of the duff reaction

Lindoy, Leonard F.,Meehan, George V.,Svenstrup, Niels

, p. 1029 - 1032 (2007/10/03)

Careful control of the reaction conditions in a modified Duff reaction using anhydrous trifluoroacetic acid as the solvent enables the selective synthesis of either 4-substituted 2-formylphenols (5-substituted salicylaldehydes) or 4-substituted 2,6-diformylphenols in one step starting from commercially available 4-substituted phenols in moderate to good yield.

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