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CAS

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77787-79-2

(Z)-2-phenyl-1,2-bis(2,4,6-trimethylphenyl)ethenol is a complex organic compound characterized by its unique molecular structure. It features a phenyl group at the 2-position, which is connected to two trimethylphenyl groups at the 1-position, forming an ethenol (vinyl alcohol) backbone. The trimethylphenyl groups are derivatives of benzene, with three methyl groups attached to each carbon atom at the 2, 4, and 6 positions. (Z)-2-phenyl-1,2-bis(2,4,6-trimethylphenyl)ethenol is known for its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its specific arrangement of functional groups and the presence of bulky substituents, it may exhibit unique reactivity and stability compared to simpler phenolic compounds.

77787-79-2

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77787-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77787-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,8 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77787-79:
(7*7)+(6*7)+(5*7)+(4*8)+(3*7)+(2*7)+(1*9)=202
202 % 10 = 2
So 77787-79-2 is a valid CAS Registry Number.

77787-79-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,2-bis(2,4,6-trimethylphenyl)-Ethenol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:77787-79-2 SDS

77787-79-2Relevant articles and documents

Vinylic Cations from Solvolysis. 42. Cyclization on Methyl, Capture by Solvent, and Degenerate Rearrangement of the Trimesitylvinyl Cation

Biali, Silvio E.,Rappoport, Zvi

, p. 964 - 970 (2007/10/02)

Trimesitylvinyl tosylate, prepared in situ from trimesitylethenol (2) and tosyl chloride, cyclizes in benzene to 2,3-dimesityl-4,6-dimethylindene (5).AgBF4-assisted reaction of trimesitylvinyl chloride (6) in the alcohols ROH, R = Me, Et, and i-Pr, gives

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