3217-15-0

Basic information

• Product Name: 4-BROMO-2.6-DICHLOROPHENOL
• Synonyms: 2,6-Dichloro-4-bromophenol;3-(1,2,3,4-tetrazol-1-yl)benzoic acid;3-(1-tetrazolyl)benzoic acid;4-Bromo-2,6-dichlorophenol, >=97%
• CAS NO: 3217-15-0
• Molecular Formula: C₆H₃BrCl₂O
• Molecular Weight: 241.89742
• EINECS: 221-740-2
• Product Categories: Phenol&Thiophenol&Mercaptan
• Mol File: 3217-15-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 64-65℃
• Boiling Point: 247℃
• Flash Point: 103℃
• Appearance: Off-white/Powder
• Density: 1.890
• Vapor Pressure: 6.96E-09mmHg at 25°C
• Refractive Index: 1.724
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• PKA: 6.46±0.23(Predicted)
• CAS DataBase Reference: 4-BROMO-2.6-DICHLOROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-2.6-DICHLOROPHENOL(3217-15-0)
• EPA Substance Registry System: 4-BROMO-2.6-DICHLOROPHENOL(3217-15-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 3217-15-0(Hazardous Substances Data)

Usage

General Description

4-Bromo-2,6-dichlorophenol is a chemical compound with the molecular formula C6H3BrCl2O. It is a white crystalline solid that is commonly used as a disinfectant and fungicide. 4-Bromo-2,6-dichlorophenol is known for its antimicrobial properties and is used in various industrial and agricultural applications. It is also used in the production of pharmaceuticals and dyes. The compound is toxic to aquatic organisms and may cause long-term adverse effects in the environment, so its use and disposal must be carefully managed to minimize potential harm.

InChI:InChI=1/C8H6N4O2/c13-8(14)6-2-1-3-7(4-6)12-5-9-10-11-12/h1-5H,(H,13,14)

Upstream product

• 106-41-2 4-bromo-phenol 
• 860725-21-9 6-bromo-2,4-dichloro-3-hydroxy-benzaldehyde 
• 7791-25-5 sulfuryl dichloride 
• 7782-50-5 chlorine 
• 64-19-7 acetic acid 
• 15719-64-9 methylammonium carbonate 
• 87-65-0 2,6-Dichlorophenol 
• 2973-80-0 2-bromo-5-hydroxybenzaldehyde 
• 7757-83-7 sodium sulfite 
• 2446-83-5 di-isopropyl azodicarboxylate 
• 4783-82-8 2-(4-bromophenyloxy)pyridine 

Downstream Products

• 618-80-4 2,6-dichloro-4-nitrophenol 
• 87-65-0 2,6-Dichlorophenol 
• 17587-86-9 4-bromo-2,4,6-trichloro-cyclohexa-2,5-dienone 
• 20244-59-1 4,4-dibromo-2,6-dichloro-cyclohexa-2,5-dienone 
• 6852-85-3 3,4,5-tribromo-2,6-dichloro-phenol 
• 19240-91-6 5-bromo-1,3-dichloro-2-methoxybenzene 
• 70123-68-1 1,3-dichloro-2-(2,6-dichloro-4-bromophenoxy)propane 
• 70123-73-8 1,2-dichloro-3-(2,6-dichloro-4-bromophenoxy)propane 
• 946-31-6 2-chloro-4,6-dinitro-phenol 
• 697-91-6 2,6-dichloro-1,4-benzoquinone 
• 525575-58-0 5-bromo-1,3-dichloro-2-(3-isopropyl-4-methoxyphenoxy)benzene 
• 383180-97-0 5-bromo-1,3-dichloro-2-(4-nitrophenoxy)-benzene 
• 957828-45-4 1,3-Dichloro-5-ethynyl-2-(4-nitro-phenoxy)-benzene 
• 383181-02-0 [4-(4-aminophenoxy)-3,5-dichloro-phenyl]-acetic acid methyl ester 

Relevant articles and documents

7-benzyl-4-(4-phenylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine derivatives and Composition for skin whitening and Pharmaceutical composition for use in preventing or treating disorders of Melanin Hyperpigmentation containing the same as an active ingredient

The present invention relates to a 7-benzyl-4(4-phenylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine derivative, and to a composition for skin whitening, comprising the same as an active ingredient. Since the derivative exhibits the effect of inhibiting the production of melanin even when used in a small amount, it is useful as a pharmaceutical composition for preventing or treating melanin hyperpigmentation diseases, a cosmetic composition for skin whitening, and a health functional food for skin whitening.

1,1,2,2-Tetrahydroperoxy-1,2-Diphenylethane: An efficient and high oxygen content oxidant in various oxidative reactions

Several oxidative approaches namely thiocyanation of aromatic compounds, epoxidation of alkenes, amidation of aromatic aldehydes, epoxidation of α β-unsaturated ketones, oxidation of sulfides to sulfoxides and sulfones, bayer-villeger reaction, bromination and iodation of aniline and phenol derivatives oxidative esterification, oxidation of pyridines and oxidation of secondary, allylic and benzyllic alcohols were carried out using 1,1,2,2-Tetrahydroperoxy-1,2-Diphenylethane as the potential solid oxidant which can be stored for several months without any loss in its activity. All of the procedures were accomplished via mild reaction conditions and the products were afforded in high yields and short reaction times.