2091-51-2

Basic information

• Product Name: 4-(bromomethyl)-2,6-ditert-butyl-phenol
• Synonyms: 2,6-Di-t-butyl-4-bromomethylphenol
• CAS NO: 2091-51-2
• Molecular Formula: C₁₅H₂₃BrO
• Molecular Weight: 299.25
• Mol File: 2091-51-2.mol
• Article Data: 19

Chemical Properties

• Melting Point: 54-55 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 308.8°Cat760mmHg
• Flash Point: 140.6°C
• Appearance: /
• Density: 1.193g/cm³
• Vapor Pressure: 0.000365mmHg at 25°C
• Refractive Index: 1.53
• PKA: 10.70±0.70(Predicted)
• CAS DataBase Reference: 4-(bromomethyl)-2,6-ditert-butyl-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(bromomethyl)-2,6-ditert-butyl-phenol(2091-51-2)
• EPA Substance Registry System: 4-(bromomethyl)-2,6-ditert-butyl-phenol(2091-51-2)

Safety Data

• Hazardous Substances Data: 2091-51-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H23BrO/c1-14(2,3)11-7-10(9-16)8-12(13(11)17)15(4,5)6/h7-8,17H,9H2,1-6H3

Upstream product

• 1669-36-9 4-bromo-4-methyl-2,6-di-tert-butylcyclohexa-2,5-dienone 
• 71-43-2 benzene 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 506-96-7 Acetyl bromide 
• 88-27-7 N,N-dimethyl-(3,5-di-tert-butyl-4-hydroxybenzyl)amine 
• 1620-98-0 3,5-di-t-butyl-4-hydroxybenzaldehyde 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 

Downstream Products

• 87-97-8 2,6-di-tert-butyl-4-methoxymethylene-phenol 
• 1516-94-5 1,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)ethane 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 
• 809-73-4 3,3',5,5'-tetra-tert-butyl-4,4'-stilbenequinone 
• 5530-31-4 2,6-di-tert-butyl-4-(3-butenyl)phenol 
• 1611-07-0 3,5-Di-tert-butyl-4-hydroxyphenylacetonitrile 
• 2607-52-5 2,6-di-tert-butyl-4-methylene-2,5-cyclohexadien-1-one 
• 78536-43-3 <3,5-di(tert-butyl)>-4-hydroxybenzylthiocyanate 
• 15367-50-7 S-3,5-di(tert-butyl)-4-hydroxybenzyl-O-ethylxanthate 
• 17258-83-2 N,N-di-ethyl-dithiocarbamic acid 3,5-di-tert-butyl-4-hydroxy-benzyl ester 
• 6029-97-6 2-[(3,5-di(tert-butyl)-4-hydroxybenzyl)sulfanyl]benzothiazole 
• 167849-33-4 3',5'-di-tert-butyltyrosine ethyl ester 
• 500695-43-2 3',5'-di-tert-butyltyrosine benzyl ester 
• 798-73-2 4-Cyclohexylaminomethyl-2.6-di-tert.-butyl-phenol 

Relevant articles and documents

With anti-oxidation function of the second carbide imine compound and its preparation method

The invention will be hindered phenol antioxidant structure and connected with the carbodiimide structure, by substitution, the coupling reaction for synthesis of molecular weight, higher melting point single carbodiimide high carbonization two imine comp

Synthesis and antimicrobial activities of phosphonium salts on basis of triphenylphosphine and 3,5-di-tert-butyl-4-hydroxybenzyl bromide

We report the structures of two new phosphonium salts prepared via the reaction of (substituted)benzyl bromides with triphenylphosphine. The antibacterial and antifungal activities are reported.

Synthesis of quaternary phosphonium salts on the basis of 2,6-di-tert-butyl-4-methylphenol

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