32703-79-0

Usage

Uses

Used in Environmental Testing and Research:
4-tert-Butylphthalic anhydride is used as a standard for environmental testing and research, providing a reliable reference for evaluating the presence and concentration of pollutants in various environmental samples.
Used in Pharmaceutical Industry:
4-tert-Butylphthalic anhydride is used as a reagent for the structure-based design of phthalimides, which are potential cyclooxygenase-2 inhibitors. These inhibitors possess anti-inflammatory and analgesic activities, making them valuable in the development of new drugs for treating pain and inflammation.
Used in Dyes and Metabolites:
4-tert-Butylphthalic anhydride is also used in the synthesis of dyes and metabolites, contributing to the development of new compounds with potential applications in various industries, including textiles, cosmetics, and pharmaceuticals.

InChI:InChI=1/C12H12O3/c1-12(2,3)7-4-5-8-9(6-7)11(14)15-10(8)13/h4-6H,1-3H3

Upstream product

• 7397-06-0 4-t-butyl-o-xylene 
• 2876-35-9 2-tert-butylnaphthalene 
• 91-20-3 naphthalene 
• 31592-22-0 2,6-di-tert-butyl-1,4-naphthoquinone 
• 3905-64-4 2,6-di-tert-butylnaphthalene 
• 95-47-6 o-xylene 
• 14236-13-6 4-(tert-butyl)phthalic acid 

Downstream Products

• 57091-50-6 dimethyl 4-(tert-butyl)phthalate 
• 106679-40-7 2-(4-tert-Butylbenzoyl)-5-tert-butylbenzoic acid 
• 855201-87-5 2-(acenaphthene-5-carbonyl)-4-tert-butyl-benzoic acid 
• 50727-07-6 4-tert-butylphthalimide 
• 374592-80-0 4-(tert-butyl)benzene-1,2-dimethanol 
• 106679-32-7 2(4-tert-Butylbenzoyl)-4-tert-butylbenzoic acid 
• 886592-55-8 4-tert-butyl-N-{2-[2-(4-methylpiperazin-1-yl)phenyl]-ethyl}-phthalamic acid 
• 886592-56-9 5-tert-butyl-N-{2-[2-(4-methylpiperazin-1-yl)phenyl]-ethyl}-phthalamic acid 
• 39001-64-4 copper (II) 2,9,16,23-tetra-tert-butyl-29H,31H-phthalocyanine 
• 14236-13-6 4-(tert-butyl)phthalic acid 
• 1293923-75-7 5-tert-butyl-2-(3,4,5-trichlorophenyl)isoindoline-1,3-dione 
• 1293923-39-3 5-tert-butyl-2-(3,4,5-trimethoxyphenyl)isoindoline-1,3-dione 

Relevant academic research and scientific papers

Synthesis of Tetrakis(4-tert-butylbenzo)porphin and its Metal Complexes

The condensation of 4-tert-butylphthalimide with sodium and zinc acetates leads to the zinc complex of tetrakis(4-tert-butylbenzo)porphin, which forms the free ligand under the influence of boiling trifluoroacetic acid.A series of metalloporphyrins were obtained from tetrakis(4-tert-butylbenzo)porphin and metal acetates.

Soluble trans-Di-1-alkynyl- and Poly-trans-ethynyl(tetraalkylphthalocyaninato)metal IVB Derivatives

The hitherto unknown peripheric substituted trans-dihalogeno(tetra-tert-butylphthalocyaninato)metal IVB derivatives 5a,b and 6a,b as well as trans-dichlorogermanium (6c) were converted into the monomeric, soluble trans-di-1-alkynyl(tetra-tert-butylphthalocyaninato)metal IVB compounds 10a - h and trans-di-1-alkynylgermanium compounds 10i - l, respectively, by the reaction with various 1-alkynyl Grignard derivatives 9a - e.The high solubility of all products in organic solvents and the strong ring-current effect of the macrocycle on the axial ligands are remarkable.The formally analogous reaction with the bidentate ethynediyldi-Grignard compound 9f leads to the soluble, acetylene-bridged polymers 12a - c.These are considered as model compounds for a new kind of one-dimensional conductors proposed by us.