3957-71-9

Basic information

• Product Name: 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL
• Synonyms: 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL
• CAS NO: 3957-71-9
• Molecular Formula: C₁₅H₂₁NOS
• Molecular Weight: 263.39834
• Mol File: 3957-71-9.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL(3957-71-9)
• EPA Substance Registry System: 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL(3957-71-9)

Safety Data

• Hazardous Substances Data: 3957-71-9(Hazardous Substances Data)

Usage

General Description

2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL is a chemical compound with the molecular formula C15H21NOS. It is a thiocyanate derivative of phenol, characterized by the presence of a thiocyanate functional group and two tert-butyl substituents on the phenol ring. 2,6-DI-TERT-BUTYL-4-THIOCYANATO-PHENOL is commonly used as a reagent in organic synthesis and chemical research. It is also used as an intermediate in the production of various compounds. In addition, it has potential pharmacological and biological activities, making it a subject of interest in pharmaceutical research. However, proper handling and safety precautions should be observed due to its potential hazards as a chemical substance.

Upstream product

• 128-39-2 2,6-di-tert-butylphenol 
• 333-20-0 potassium thioacyanate 
• 2290-65-5 trimethylsilyl isothiocyanate 
• 540-72-7 sodium thiocyanide 

Downstream Products

• 950-59-4 4-hydroxy-3,5-di-tert-butylthiophenol 
• 6386-58-9 4,4'-dithiobis(2,6-di-tert-butylphenol) 
• 84161-18-2 2,6-Di-tert-butyl-4-(methylsulfonyl)phenol 
• 55485-65-9 <1-Hydroxy-2,6-di-tert.-butyl-phenyl-(4)>-essigsaeurethiolester 
• 94092-37-2 2,6-bis(1,1-dimethylethyl)-4-(methylsulfinyl)phenol 
• 26532-81-0 4-tert.-Butylmercapto-2,6-di-tert.-butyl-phenol 
• 26532-80-9 2,6-di-tert-butyl-4-(methylsulfanyl)phenol 
• 4673-51-2 4,4'-thiobis[2,6-bis(tert-butyl)phenol] 
• 169180-32-9 2-amino-6-(3,5-di-tert-butyl-4-hydroxyphenylthio)-4-trichloromethyl-sym-triazine 
• 162933-23-5 6-<3,5-di(tert-butyl)-4-hydroxyphenylthio>-2,4-bis(trichloromethyl)-sym-triazene 
• 2444-28-2 2,6-di-tert-butyl-4-hydroxyphenol 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 
• 81056-41-9 7-tert-Butyl-2-methyl-5-thiocyanatobenzoxazol 
• 105648-50-8 2,4,6-tris(4-hydroxy-3,5-di-tert-butylphenylthio)-symm-triazine 

Relevant articles and documents

Synthesis method of dithiobis-butyl phenol and analogue thereof

The invention provides a synthesis method of dithiobis-butyl phenol and an analogue thereof. The synthesis method provided by the invention has the advantages of few steps, high yield and high purity of the obtained product. The dithiobis-butyl phenol and the analogue thereof synthesized by the invention can be used for preparing medicines for preventing and/or treating coronavirus pneumonia (containing COVID-19).

Probucol derivative, preparation method and application thereof

The invention relates to the fields of compounds, and specifically relates to a probucol derivative, a preparation method and the application thereof. The probucol derivative has a structure shown asa general formula I. The probucol derivative provided by the invention can be used for prevention and curing of vascular diseases such as diabetes and cardiovascular and cerebrovascular diseases or complications thereof, can be used for reducing blood glucose, reducing blood fat, reducing cholesterol, reducing the weight, reducing triglyceride, resisting inflammation and oxidation and the like effectively, and has a wide application prospect.

2-AMINOETHANESULFONIC ACID DERIVATIVES OF 3,5-DISUBSTITUTED-4-HYDROXY-PHENOLIC THIOETHERS

The present invention relates to compounds of the Formula I:wherein R1 and R2 are the same or different and independently represent tert-alkyl, halogen, or phenyl; Alk 1 represents straight or branched chain alkylene of 2 to 10 carbon atoms which can optionally be substituted by hydroxy, provided that said hydroxy is not attached to a carbon which is adjacent to sulfur or oxygen, X represents sulfur or oxygen, and Alk 2 represents straight or branched chain alkylene of 1 to 4 carbon atoms; and the pharmaceutically acceptable salts thereof. These compounds are specific 5-lipoxygenase inhibitors and are useful as anti-inflammatory and anti-allergy agents and in the treatment of conditions mediated by 5-lipoxygenase