50419-88-0

Basic information

• Product Name: BUTTPARK 80\07-66
• Synonyms: BUTTPARK 80\07-66;2-AMINO-5-BROMO-4-CHLOROBENZOIC ACID;4-Chloro-5-bromoanthranilic acid;2-amino-5-bromo-4-chlorobenzene carboxylic acid;BENZOIC ACID, 2-AMINO-5-BROMO-4-CHLORO-
• CAS NO: 50419-88-0
• Molecular Formula: C₇H₅BrClNO₂
• Molecular Weight: 250.48
• Mol File: 50419-88-0.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Density: 1.892
• CAS DataBase Reference: BUTTPARK 80\07-66(CAS DataBase Reference)
• NIST Chemistry Reference: BUTTPARK 80\07-66(50419-88-0)
• EPA Substance Registry System: BUTTPARK 80\07-66(50419-88-0)

Safety Data

• Hazardous Substances Data: 50419-88-0(Hazardous Substances Data)

Usage

Description

BUTTPARK 80\07-66 is a proprietary chemical blend that functions as a corrosion inhibitor and surfactant, specifically formulated to protect metal surfaces from oxidation and corrosion in aqueous environments. Its unique composition of organic compounds also enhances the wetting and spreading of liquids, making it an effective ingredient in cleaning agents and industrial coatings. Renowned for its high performance and versatility, BUTTPARK 80\07-66 is a popular choice across various industries for its ability to improve the efficiency and longevity of metal surfaces.

Uses

Used in Chemical Industry:
BUTTPARK 80\07-66 is used as a corrosion inhibitor for protecting metal surfaces from oxidation and corrosion, particularly in aqueous environments. Its application helps to extend the life of metal equipment and reduce maintenance costs.
Used in Cleaning Agents:
BUTTPARK 80\07-66 is used as a surfactant in the formulation of cleaning agents to improve the wetting and spreading of liquids. This enhances the cleaning efficiency and effectiveness of the agents, leading to better overall performance.
Used in Industrial Coatings:
BUTTPARK 80\07-66 is used as an additive in industrial coatings to enhance the wetting and spreading of the coating on metal surfaces. This results in a more uniform and durable coating, providing better protection and corrosion resistance.
Used in Oil and Gas Industry:
BUTTPARK 80\07-66 is used as a corrosion inhibitor in the oil and gas industry to protect pipelines and other metal infrastructure from the corrosive effects of water and other substances. This helps to maintain the integrity of the infrastructure and prevent leaks and failures.
Used in Automotive Industry:
BUTTPARK 80\07-66 is used as a corrosion inhibitor in automotive applications to protect metal components from oxidation and corrosion, ensuring the longevity and performance of the vehicle. It is also used in the formulation of automotive coatings to provide a durable and protective finish.
Used in Marine Industry:
BUTTPARK 80\07-66 is used as a corrosion inhibitor in marine applications to protect metal components of ships, boats, and offshore structures from the corrosive effects of saltwater and other harsh marine environments. This helps to maintain the structural integrity and performance of these components.
Used in Manufacturing Industry:
BUTTPARK 80\07-66 is used as a corrosion inhibitor and surfactant in various manufacturing processes to protect metal tools, equipment, and machinery from corrosion and improve the efficiency of cleaning and coating processes. This contributes to increased productivity and reduced downtime in manufacturing operations.

Upstream product

• 1607828-44-3 N-acetyl-5-bromo-4-chloroanthranilic acid 
• 5900-55-0 N-(5-chloro-2-methylphenyl)acetamide 
• 1607828-43-2 N-(4-bromo-5-chloro-2-methylphenyl)-acetamide 
• 89-77-0 2-Amino-4-chlorobenzoic acid 

Downstream Products

• 1607828-49-8 5-bromo-4-chloro-N-[(allyloxycarbonyl)methyl]anthranilic acid allyl ester 
• 93863-88-8 (5-bromo-6-chloroindol-3-yl)-β-D-galactopyranoside 
• 103029-90-9 N-(4-bromo-5-chloro-2-carboxy)phenylglycine 
• 108847-96-7 1-acetyl-5-bromo-6-chloro-1H-indol-3-yl acetate 
• 1036757-11-5 2-amino-5-bromo-4-chlorobenzaldehyde 
• 1036757-10-4 (2-amino-5-bromo-4-chlorophenyl)methanol 
• 1621669-61-1 C₃₈H₁₈BrClN₂ 
• 1621669-62-2 C₃₈H₁₈BrClN₂ 
• 1621669-56-4 C₅₂H₂₆N₂ 
• 1621669-57-5 C₅₂H₂₆N₂ 
• 1621669-63-3 C₅₂H₂₇ClN₂ 
• 1621669-64-4 C₅₂H₂₇ClN₂ 
• 1616955-04-4 (Z)-tert-butyl (2-(4-bromo-5-chloro-2-formylstyryl)phenyl)carbamate 
• 1616954-94-9 tert-butyl (2-((4-bromo-5-chloro-2-(hydroxymethyl)phenyl)ethynyl)phenyl)carbamate 

Relevant articles and documents

QUINOLINO-PYRROLIDIN-2-ONE DERIVATIVE AND APPLICATION THEREOF

Disclosed are a series of quinolino-pyrrolidin-2-one compounds, and application thereof in preparation of drugs for ATM inhibitor-related diseases. The present disclosure specifically relates to a derivative compound represented by formula (I), tautomers thereof or pharmaceutically acceptable compositions thereof.

A 5 - bromo - 4 - chloro - 2 - amino preparation method of acetophenone (by machine translation)

The invention discloses a 5 - bromo - 4 - chloro - 2 - amino acetophenone preparation method, the method comprises the following steps: to 4 - chloro - 2 - aminobenzoic acid as the starting material, the reaction of halide 5 - bromo - 4 - chloro - 2 - ami

Indoxylic acid esters as convenient intermediates towards indoxyl glycosides

Indoxylic acid methyl and allyl esters with varied halide-substitution patterns were obtained in excellent yields using a scalable route. Phase-transfer glycosylation of these key intermediates was carried out with various glycosyl halides. Subsequent mild silver-mediated decarboxylation followed by Zemplen deacetylation led to indoxyl glycosides in good overall yields. Indoxyl glycosides are well-established and widely used tools for enzyme screening and enzyme-activity monitoring. In the past, their synthesis has been difficult, so this new approach has led to a variety of useful structures. Indoxyl glycosides with varied halide-substitution patterns were synthesized using indoxylic acid esters as key intermediates. Glycosylation under phase-transfer conditions, ester cleavage, and mild decarboxylation led to the indoxyl glycosides in good yields. This approach enables access to a number of different indoxyl compounds. Copyright