CAS 20834-61-1

2-Bromo-4,6-di-tert-butylphenol

Description:

2-Bromo-4,6-di-tert-butylphenol is an organic compound characterized by its phenolic structure, which includes a bromine atom and two tert-butyl groups attached to the aromatic ring. The presence of the bromine substituent enhances its reactivity, while the bulky tert-butyl groups contribute to its steric hindrance, influencing its physical and chemical properties. This compound typically appears as a solid at room temperature and is known for its antioxidant properties, making it useful in various industrial applications, particularly in plastics and rubber formulations to prevent oxidative degradation. Its molecular structure also suggests potential applications in pharmaceuticals and agrochemicals. The compound is generally stable under standard conditions but may undergo reactions typical of phenolic compounds, such as electrophilic substitution or oxidation. Safety data indicates that, like many brominated compounds, it should be handled with care due to potential toxicity and environmental concerns. Proper safety measures, including the use of personal protective equipment, are recommended when working with this substance.

Formula: C₁₄H₂₁BrO

InChI: InChI=1/C14H21BrO/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8,16H,1-6H3

InChI key: InChIKey=DIWZVAHZEOFSLS-UHFFFAOYSA-N

SMILES: C(C)(C)(C)C1=CC(C(C)(C)C)=CC(Br)=C1O

Synonyms:

• 2-Bromo-4,6-bis(1,1-dimethylethyl)phenol
• 2-Bromo-4,6-bis(tert-butyl)phenol
• 2-Bromo-4,6-di-t-butylphenol
• 2-Bromo-4,6-ditert-butylphenol
• 4,6-Di(tert-butyl)-2-bromophenol
• 6-Bromo-2,4-tert-butylphenol
• Phenol, 2-Bromo-4,6-Bis(1,1-Dimethylethyl)-
• Phenol, 2-bromo-4,6-di-tert-butyl-
• 2-Bromo-4,6-di-tert-butylphenol
• 2-BROMO-4,6-DI-TERT-BUTYLPHENOL
• AKOS GLO-BB-408

2-Bromo-4,6-di-tert-butylphenol, 97%

CAS: 20834-61-1

It is used in pharmaceutical intermediates and as medicine. When 2-Bromo-4,6-di-tert-butylphenol was treated with potassium ferricyanide in benzene 1,4-dihydro-4-bromo-2,4,6,8-tetra-tert-butyl-1-oxodibenzofuran was yielded with a small amount of 2,4,6,8-tetra-tert-butyldibenzofuran. This Thermo S

Formula: C₁₄H₂₁BrO

Purity: 97%

Color and Shape: White to cream or yellow to orange, Crystals or powder or crystalline powder or lumps

Molecular weight: 285.23

Ref: 02-A13218

Phenol, 2-bromo-4,6-bis(1,1-dimethylethyl)-

CAS: 20834-61-1

Formula: C₁₄H₂₁BrO

Purity: 97%

Color and Shape: Solid

Molecular weight: 285.2199

Ref: IN-DA002JNB

2,4-Bis(tert-butyl)-6-bromophenol

CAS: 20834-61-1

2,4-Bis(tert-butyl)-6-bromophenol

Formula: C₁₄H₂₁BrO

Purity: 97%

Color and Shape: white to off-white crystalline solid

Molecular weight: 285.22g/mol

Ref: 54-OR21276

2-Bromo-4,6-di-tert-butylphenol

CAS: 20834-61-1

Formula: C₁₄H₂₁BrO

Purity: 97%

Molecular weight: 285.225

Ref: 10-F336697

2,4-Bis(tert-butyl)-6-bromophenol

CAS: 20834-61-1

2,4-Bis(tert-butyl)-6-bromophenol (2,4-BBP) is a ligand that binds to copper and forms an electron transfer complex. It has been shown to form radical species in the presence of proton and hydrogen. The crystal structure of the copper complex has been determined by x-ray diffraction. The ligand can be debrominated with electrochemical methods and the resulting product can be identified by nmr spectroscopy or absorption spectroscopy. The phenoxy group is well known for its ability to form a thiolate bond with hydrogen peroxide. 2,4-BBP has also been shown to have metal ion binding properties as well as anti-inflammatory activities.

Formula: C₁₄H₂₁BrO

Purity: Min. 95%

Molecular weight: 285.22 g/mol

Ref: 3D-VAA83461