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CAS

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51806-71-4

Phenol, 2,6-bis(1,1-dimethylethyl)-4-(oxiranylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 51806-71-4 Structure

  • Basic information

    1. Product Name: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(oxiranylmethyl)-
    2. Synonyms:
    3. CAS NO:51806-71-4
    4. Molecular Formula: C17H26O2
    5. Molecular Weight: 262.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51806-71-4.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: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(oxiranylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(oxiranylmethyl)-(51806-71-4)
    11. EPA Substance Registry System: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(oxiranylmethyl)-(51806-71-4)

  • 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: 51806-71-4(Hazardous Substances Data)

51806-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51806-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,0 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51806-71:
(7*5)+(6*1)+(5*8)+(4*0)+(3*6)+(2*7)+(1*1)=114
114 % 10 = 4
So 51806-71-4 is a valid CAS Registry Number.

51806-71-4Relevant articles and documents

β-Hydroxyalkylation of sterically hindered phenols with epoxides in acid medium

Krysin,Amitina,Egorova,Vasiliev

experimental part, p. 354 - 360 (2011/06/27)

Reactions of 2,6-dialkylphenols with ethylene oxide, propylene oxide and epichlorohydrin in the presence of SnCl4 at the temperature from -5 to +5°C leads to the formation of respective phenols containing a hydroxy group in the β-position of the aliphatic chain of the para-substituent. The conditions for maximum selectivity of the reaction of 2,6-di-tert-butylphenol with ethylene oxide were determined. By HPLC-MS method the directions of the side reactions were explored. The method has been successfully tested in a pilot installation. With 2,6-dimethylphenol instead of 2,6-di-tert-butylphenol a sharp increase occurs in the content of ethers in the reaction product. With epichlorohydrin, 2,6-di-tert-butylphenol affords a product, which is easily converted into an epoxide containing a sterically hindered phenol in its structure.

3,5-DIALKYL-4-HYDROXYBENZYL-OXIRANES

-

, (2008/06/13)

New 3,5-dialkyl-4-hydroxybenzyl-oxiranes and the corresponding thiiranes are used as stabilizers for polymers. The oxiranes are prepared from the corresponding olefins by reaction with percarboxylic acids or from alkali phenoxides and epichlorohydrines. T

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