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4-methyl-2-(2,4,4-trimethylpentan-2-yl)phenol is a complex organic compound with the molecular formula C16H26O. It is a derivative of phenol, characterized by a methyl group at the 4th position and a bulky 2,4,4-trimethylpentan-2-yl substituent attached to the 2nd position. 4-methyl-2-(2,4,4-trimethylpentan-2-yl)phenol is known for its unique structure and potential applications in various chemical and industrial processes. Due to its specific molecular arrangement, it may exhibit distinct chemical properties and reactivity compared to simpler phenol derivatives. The compound's structure and properties make it a subject of interest for researchers in organic chemistry, particularly in the development of new materials and compounds with specialized functions.

4979-46-8

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4979-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4979-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4979-46:
(6*4)+(5*9)+(4*7)+(3*9)+(2*4)+(1*6)=138
138 % 10 = 8
So 4979-46-8 is a valid CAS Registry Number.

4979-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-(2,4,4-trimethylpentan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-tert-octylphenol

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4979-46-8 SDS

4979-46-8Relevant academic research and scientific papers

ALKYLATION OF HYDROXYARENES WITH OLEFINS, ALCOHOLS AND ETHERS IN IONIC LIQUIDS

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Page/Page column 25, (2008/06/13)

Hydroxyarenes are alkylated using an ionic liquid catalyst system with olefins, alcohols, or ethers as alkylating agents. The ionic liquid catalyst system comprises chloroindate (III) anions. The reactions may be conducted at moderate temperatures and pressures to yield commercially relevant alkylated hydroxyarene compounds.

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