154532-34-0

Basic information

• Product Name: BUTTPARK 148\01-24
• Synonyms: BUTTPARK 148\01-24;3-TERT-BUTYL-BENZONITRILE;3-(1,1-Dimethylethyl)benzonitrile
• CAS NO: 154532-34-0
• Molecular Formula: C₁₁H₁₃N
• Molecular Weight: 159.23
• Mol File: 154532-34-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 238℃
• Flash Point: 98℃
• Appearance: /
• Density: 0.95
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: BUTTPARK 148\01-24(CAS DataBase Reference)
• NIST Chemistry Reference: BUTTPARK 148\01-24(154532-34-0)
• EPA Substance Registry System: BUTTPARK 148\01-24(154532-34-0)

Safety Data

• Hazardous Substances Data: 154532-34-0(Hazardous Substances Data)

Usage

General Description

BUTTPARK 148\01-24 is a chemical blend designed for use in the production of rubber goods such as tires, conveyor belts, and other industrial rubber products. It is a vulcanization accelerator that helps to improve the physical and mechanical properties of rubber, increasing its strength and resilience. The specific composition of this blend is proprietary, but it likely contains chemicals such as accelerators, antioxidants, and other additives that help to improve the overall performance of rubber products. Overall, BUTTPARK 148\01-24 is designed to enhance the processing and performance of rubber materials in various industrial applications.

Upstream product

• 253185-03-4 tert-butylbenzene 
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• 623-00-7 4-bromobenzenecarbonitrile 
• 865-47-4 potassium tert-butylate 
• 71-43-2 benzene 
• 585-34-2 3-tert-butylphenyol 
• 557-21-1 zinc(II) cyanide 
• 201851-06-1 m-(tert-butyl)phenyl trifluoromethanesulfonate 
• 626-17-5 benzene-1,3-dicarbonitrile 
• 1184-88-9 sodium pivalate 
• 85-01-8 phenanthrene 
• 460-19-5 ethanedinitrile 
• 3972-64-3 1-bromo-3-(tertbutyl)benzene 
• 557-21-1 dicyanozinc 

Downstream Products

• 7498-54-6 3-t-Butylbenzoic acid 
• 1385069-07-7 tert-butyl 3-(tert-butyl)benzylcarbamate 
• 1385067-81-1 N-((E)-(S)-4-[(R)-2-(3-tert-butyl-benzylamino)-1-hydroxy-ethyl]-2,13-dioxo-6-oxa-3,12-diaza-bicyclo[12.3.1]octadeca-1⁽¹⁷⁾,8,14⁽¹⁸⁾,15-tetraen-16-yl)-N-methyl-methanesulfonamide 
• 900802-72-4 1-(3-tert-butyl-phenyl)-cyclo-propylamine 
• 608515-16-8 (3-(tert-butyl)phenyl)methanamine 
• 140401-55-4 3-tert-Butyl-benzylamine; hydrochloride 

Relevant articles and documents

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Dual Ligand-Enabled Nondirected C-H Cyanation of Arenes

Aromatic nitriles are key structural units in organic chemistry and, therefore, highly attractive targets for C-H activation. Herein, the development of an arene-limited, nondirected C-H cyanation based on the use of two cooperatively acting commercially available ligands is reported. The reaction enables the cyanation of arenes by C-H activation in the absence of directing groups and is therefore complementary to established approaches.

Ligand-Promoted Non-Directed C?H Cyanation of Arenes

This article reports the first example of a 2-pyridone accelerated non-directed C?H cyanation with an arene as the limiting reagent. This protocol is compatible with a broad scope of arenes, including advanced intermediates, drug molecules, and natural products. A kinetic isotope experiment (kH/kD=4.40) indicates that the C?H bond cleavage is the rate-limiting step. Also, the reaction is readily scalable, further showcasing the synthetic utility of this method.