24676-69-5

Basic information

• Product Name: potassium 2,6-di-tert-butylphenolate
• Synonyms: potassium 2,6-di-tert-butylphenolate;Potassium 2,6-bis(1,1-dimethylethyl)phenolate;Einecs 246-397-6;Phenol, 2,6-bis(1,1-dimethylethyl)-, potassium salt;Phenol, 2,6-bis(1,1-dimethylethyl)-, potassium salt (1:1)
• CAS NO: 24676-69-5
• Molecular Formula: C₁₄H₂₁KO
• Molecular Weight: 244.41424
• EINECS: 246-397-6
• Mol File: 24676-69-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 251.4°Cat760mmHg
• Flash Point: 118.3°C
• Appearance: /
• Density: 0.932g/cm³
• CAS DataBase Reference: potassium 2,6-di-tert-butylphenolate(CAS DataBase Reference)
• NIST Chemistry Reference: potassium 2,6-di-tert-butylphenolate(24676-69-5)
• EPA Substance Registry System: potassium 2,6-di-tert-butylphenolate(24676-69-5)

Safety Data

• Hazardous Substances Data: 24676-69-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H22O.K/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6;/h7-9,15H,1-6H3;/q;+1/p-1

Upstream product

• 128-39-2 2,6-di-tert-butylphenol 

Downstream Products

• 129708-81-2 4-(3',5'-di-tert-butyl-4'-hydroxyphenyl)pyridine 
• 114460-18-3 5-cyano-2-(3',5'-di-tert-butyl-4'-hydroxyphenyl)pyridine 
• 128-39-2 2,6-di-tert-butylphenol 
• 14798-26-6 picrate anion 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 167696-49-3 Th(Br)2(OC₆H₃(C(CH₃)3)2)2(C₄H₈O)2 
• 173916-44-4 Th(OC₆H₃(C(CH₃)3)2)2(CH₂Si(CH₃)3)(OC(NC₆H₃(CH₃)2)CH₂Si(CH₃)3) 
• 173916-45-5 Th(OC₆H₃(C(CH₃)3)2)2(NHC₆H₃(CH(CH₃)2)2)2 
• 6386-38-5 methyl 3-(4-hydroxy-3,5-di-tert-butyl)phenylpropanoate 
• 36913-60-7 bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyloxymethyl]bis(hydroxymethyl)methane 
• 84633-54-5 tris[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyloxymethyl](hydroxymethyl)methane 
• 618-48-4 3-chlorobenzamide 
• 619-56-7 4-chlorobenzamide 

Relevant articles and documents

ELECTROSYNTHESIS OF UNSYMMETRICAL BIARYLS USING A SRN1 TYPE REACTION

A new synthetic route to unsymmetrical biaryls is described, involving an electrochemically induced chain reaction of the SRN1 type.

Preparation method of 2,6-ditert-butyl phenol salt

The invention provides a preparation method of 2,6-ditert-butyl phenol salt. The preparation method comprises the following steps: carrying out reflux dehydration reaction on 2,6-ditert-butyl phenol and an alkali metal compound in a molar ratio of (1 to 1)-(1 to 1.4) in a benzene solvent under the protection of inert gas; and after the reaction is finished, cooling and filtering under the protection of inert gas, and carrying out vacuum drying, so as to obtain an off-white solid product, namely the 2,6-ditert-butyl phenol salt. According to the preparation method, by carrying out reflux dehydration by virtue of the benzene solvent, the reaction process is accelerated, the reaction time is shortened, and the synthetic efficiency of the 2,6-ditert-butyl phenol salt is improved; the benzene solvent is capable of taking away unreacted raw materials and generated impurities in a post-treatment filtration process, so that the product purity is increased; the prepared 2,6-ditert-butyl phenol salt is an off-white product, high in quality and wide in use range; and the protection of inert gas is implemented in the reaction process and the post-treatment process, so that air can be effectively isolated, the production of byproducts is reduced, and the yield of the 2,6-ditert-butyl phenol salt is increased.