125023-51-0

Basic information

• Product Name: 1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]-
• CAS NO: 125023-51-0
• Molecular Formula: C18H16N2O
• Molecular Weight: 276.338
• Mol File: 125023-51-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]-(125023-51-0)
• EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]-(125023-51-0)

Safety Data

• Hazardous Substances Data: 125023-51-0(Hazardous Substances Data)

Usage

General Description

1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]- is a chemical compound consisting of a benzene ring with two cyano groups and a 4-[4-(1,1-dimethylethyl)phenoxy] substituent. It is also known as Terbutryn, and is commonly used as a herbicide to control unwanted vegetation in agricultural and non-agricultural settings. This chemical is considered to be relatively low in acute toxicity to mammals, but may pose a risk to aquatic organisms and bees. Additionally, it has been classified as a potential endocrine disruptor. Due to its potential ecological and health impacts, the use and handling of 1,2-Benzenedicarbonitrile, 4-[4-(1,1-dimethylethyl)phenoxy]- should be carefully regulated and monitored.

Upstream product

• 98-54-4 para-tert-butylphenol 
• 31643-49-9 4-Nitrophthalonitrile 
• 13138-53-9 4-nitrophthalic amide 

Downstream Products

• 210057-16-2 [zinc(tetra(tert-butyl-phenoxy)phthalocyanine)] 
• 115373-25-6 tetra-β-(4-tert-butylphenoxy)phthalocyanine 
• 125023-52-1 6-(p-tert-butylphenoxy)-1,3-dihydro-1,3-diiminoisoindole 

Relevant articles and documents

Phosphorous tetrabenzocorrolazine from its metal-free phthalocyanine precursor: Its facile synthesis, high fluorescence emission, efficient singlet oxygen formation, and promising hole transporting material

We have synthesized tetra(4-tert-butyl phenoxy)-tetrabenzocorrolazine phosphorous POTBC(β-OPB)4, a functional π-conjugated macrocycle compound derived from corrole or corrolazine, by a one step procedure from its metal free phthalocyanine precu

Al(III) phthalocyanine catalysts for CO2 addition to epoxides: Fine-tunable selectivity for cyclic carbonates versus polycarbonates

A sustainable synthetic methodology to prepare bifunctional cationic imidazolyl and neutral tert-butylphenoxy Al(III)-phthalocyanine complexes is described, using ultrasound irradiation to synthesize the phthalonitrile precursors, followed by microwave-as

Synthesis, photophysical and photochemical properties of aryloxy tetra-substituted gallium and indium phthalocyanine derivatives

The synthesis, photophysical and photochemical properties of the tetra-substituted aryloxy gallium(III) and indium(III) phthalocyanines are reported for the first time. General trends are described for photodegradation, singlet oxygen, fluorescence, and t

Enhanced photocatalytic activity in metal phthalocyanine-sensitized TiO2 nanorods

Two novel metal phthalocyanines (Zn Tetra(butylformate-phenoxy)phthalocyanine (ZnTBPP) and Zn Tetra(tert-butyl-phenoxy)phthalocyanine (ZnTTPP)) were synthesized. Besides, TiO2 nanorods (PN) are prepared through the hydrothermal method. The synt