40056-43-7

Basic information

• Product Name: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-
• Synonyms: 4-hydroxy-3,5-di-tert-butylbenzoyl chloride;3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoylchloride;Benzoyl chloride,3,5-bis(1,1-dimethylethyl)-4-hydroxy;3,5-di-(1,1dimethylethyl)-4-hydroxybenzoyl chloride;3,5-di-tert-butyl-4-hydroxy-benzoyl chloride;3,5-bis(t-butyl)-4-hydroxybenzoyl chloride
• CAS NO: 40056-43-7
• Molecular Formula: C15H21ClO2
• Molecular Weight: 268.784
• Mol File: 40056-43-7.mol
• Article Data: 28

Chemical Properties

• Melting Point: 94 °C
• Boiling Point: 327.4±42.0 °C(Predicted)
• Density: 1.085±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-(40056-43-7)
• EPA Substance Registry System: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-(40056-43-7)

Safety Data

• Hazardous Substances Data: 40056-43-7(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 1421-49-4 3,5-Di-tert-butyl-4-hydroxybenzoic acid 

Downstream Products

• 130116-76-6 1,1-dimethyl 2-<3,5-bis(1,1-dimethyl)-4-hydroxybenzoyl>hydrazinecarboxylate 
• 29078-05-5 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-methoxybenzoxazole 
• 15433-76-8 3,5-di-tert-butyl-2',4,4'-trihydroxybenzophenone 
• 69425-13-4 R₈₃₀ 
• 94253-63-1 4-Hydroxy-3.5-di-tert-butyl-benzoesaeure-isopropylester 
• 2511-22-0 methyl 3,5-di-tert-butyl-4-hydroxybenzoate 
• 82051-38-5 2,6-Di-tert-butyl-4-(5-nitro-benzooxazol-2-yl)-phenol 
• 29078-07-7 2,6-di-tert-butyl-4-(5-chloro-benzooxazol-2-yl)-phenol 
• 69442-04-2 N-methyl-3,5-di tert-butyl-4-hydroxybenzamide 
• 29219-64-5 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-methylbenzoxazole 
• 29078-14-6 2-(3,5-di-tert-butyl-4-hydroxyphenyl)benzothiazole 
• 121613-49-8 N-phenyl-3,5-di-tert-butyl-4-hydroxybenzamide 
• 121613-51-2 3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-(4-nitrophenyl)-benzamide 
• 50910-51-5 3,5-di-tert-butyl-4-hydroxy-N-phenylbenzohydroxamic acid 

Relevant articles and documents

Novel organotin complexes with phenol and imidazole moieties for optimized antitumor properties

A series of novel imidazole-containing ligands and their organotin complexes were synthesized and characterized by NMR, IR, MALDI and elemental analysis. Redox behavior was studied by cyclic voltammetry (CV). Antioxidant properties were estimated in model

Novel diphenylsulfimide antioxidants containing 2,6-di-tert-butylphenol moieties

New diphenylsulfimide derivatives containing substituents with the 2,6-di-tert-butylphenol moiety at the nitrogen atom were synthesized. Their molecular structures were established by X-ray diffraction. Antioxidant activity was experimentally evaluated by spectrophotometry based on hydrogen transfer to the stable radicals, namely, 2,2-diphenyl-1-picrylhydrazyl and the 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation (ABTS·+), and using in vitro lipid peroxidation in rat brain and liver homogenates. The presence of phenol and diphenylsulfimide moieties in one molecule leads to a significant enhancement of antioxidant activity. The new compounds exhibit moderate inhibitory activity against enzymes involved in carbohydrate and lipid metabolism. The evaluation of antiglycation activity showed that the new sulfimides taken at a concentration of 100 μmol L–1 have activity comparable with that of aminoguanidine.

NOVEL GLUCOPYRANOSE DERIVATIVES, PREPARATION THEREOF, AND BIOLOGICAL USES THEREOF

The invention relates to a novel ester, the 3,5-di-tertiobutyl-4-hydroxybenzoate of 3,4,5-trihydroxy-6-methoxytetrahydropyran-2-yl methyl defined by the following formula (I). The invention also relates to the method for preparing the compound of formula