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2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59778-96-0

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59778-96-0 Usage

Chemical class

Antioxidant

Appearance

Solid, white powder

Molecular weight

490.7 g/mol

Functionality

Inhibits oxidation in polymers, plastics, and rubber

Purpose

Prevents degradation from exposure to heat and light

Benefits

Extends lifespan and maintains mechanical properties of materials

Additional uses

Stabilizer in adhesives, coatings, and lubricants

Check Digit Verification of cas no

The CAS Registry Mumber 59778-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59778-96:
(7*5)+(6*9)+(5*7)+(4*7)+(3*8)+(2*9)+(1*6)=200
200 % 10 = 0
So 59778-96-0 is a valid CAS Registry Number.

59778-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-[(2,4,6-trimethylphenyl)methyl]phenol

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert-butyl-4-(2,4,6-trimethylbenzyl)phenol

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:59778-96-0 SDS

59778-96-0Downstream Products

59778-96-0Relevant academic research and scientific papers

Electrophotocatalytic Undirected C?H Trifluoromethylations of (Het)Arenes

Qiu, Youai,Scheremetjew, Alexej,Finger, Lars H.,Ackermann, Lutz

supporting information, p. 3241 - 3246 (2020/02/27)

Electrophotochemistry has enabled arene C?H trifluoromethylation with the Langlois reagent CF3SO2Na under mild reaction conditions. The merger of electrosynthesis and photoredox catalysis provided a chemical oxidant-free approach for the generation of the CF3 radical. The electrophotochemistry was carried out in an operationally simple manner, setting the stage for challenging C?H trifluoromethylations of unactivated arenes and heteroarenes. The robust nature of the electrophotochemical manifold was reflected by a wide scope, including electron-rich and electron-deficient benzenes, as well as naturally occurring heteroarenes. Electrophotochemical C?H trifluoromethylation was further achieved in flow with a modular electro-flow-cell equipped with an in-operando monitoring unit for on-line flow-NMR spectroscopy, providing support for the single electron transfer processes.

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