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4-benzyloxy-3-t-butylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85969-40-0 Structure
  • Basic information

    1. Product Name: 4-benzyloxy-3-t-butylphenol
    2. Synonyms:
    3. CAS NO:85969-40-0
    4. Molecular Formula:
    5. Molecular Weight: 256.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85969-40-0.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: 4-benzyloxy-3-t-butylphenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyloxy-3-t-butylphenol(85969-40-0)
    11. EPA Substance Registry System: 4-benzyloxy-3-t-butylphenol(85969-40-0)
  • 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: 85969-40-0(Hazardous Substances Data)

85969-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85969-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85969-40:
(7*8)+(6*5)+(5*9)+(4*6)+(3*9)+(2*4)+(1*0)=190
190 % 10 = 0
So 85969-40-0 is a valid CAS Registry Number.

85969-40-0Relevant articles and documents

HYDROQUINONE DERIVATIVES

-

, (2008/06/13)

A hydroquinone derivative useful as an intraocular pressure lowering, anti-hypertensive and radical scavenging agent represented by the following formula wherein B1 and B2 in formula (I) are the same or different and at any position on the benzene ring (when W is nitrogen, however, at any other position on the benzene ring) and each denotes a substituent selected from the group consisting of hydrogen, halogen, hydroxyl, lower alkoxyl and carboxyl, and the substituent CH3 is at position 2 or 3, and W are the same or different and each denotes a nitrogen or carbon atom. R1, R2, R3 and R4 in formula (II) are the same or different and each denotes a substituent selected from the group consisting of hydrogen, lower alkyl and lower alkoxyl, and B1 and B2 are as hereinbefore defined, or a pharmacologically acceptable salt thereof.

Oxidation of Alkoxyphenols. Part 28. On the Configuration of 2,2'-Diphenoquinones

Hewgill, Frank R.,Greca, Bart La,Legge, Frank,Roga, Peter E.

, p. 131 - 134 (2007/10/02)

The n.m.r. spectra of a number of 2,2'-diphenoquinones imply that they have the trans-configuration.The importance of charge-separated structures in unsymmetrical quinones is discussed in relation to the formation of oxepinobenzofurans.

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