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

General Description

BUTTPARK 80\07-66 is a chemical blend used as a corrosion inhibitor and surfactant in various industrial applications. It is a proprietary mixture of organic compounds designed to protect metal surfaces from oxidation and corrosion, especially in aqueous environments. This blend is also used to improve the wetting and spreading of liquids, making it useful in the formulation of cleaning agents and industrial coatings. BUTTPARK 80\07-66 is known for its high performance and versatility, making it a popular choice for a wide range of industries and applications.

Upstream product

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

Downstream Products

• 1166378-30-8 6-bromo-7-chloroquinazoline-2,4(1H,3H)-dione 
• 1422032-64-1 C₃₂H₁₈BrCl 
• 1443008-73-8 C₄₈H₂₆BrCl 
• 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 
• 1616954-99-4 (Z)-tert-butyl (2-(4-bromo-5-chloro-2-(hydroxymethyl)styryl)phenyl)carbamate 
• 1539228-96-0 5-bromo-4-chloro-2-iodobenzoic acid 
• 1616954-89-2 (2-((2-aminophenyl)ethynyl)-5-bromo-4-chlorophenyl)methanol 
• 1616954-94-9 tert-butyl (2-((4-bromo-5-chloro-2-(hydroxymethyl)phenyl)ethynyl)phenyl)carbamate 
• 1616955-04-4 (Z)-tert-butyl (2-(4-bromo-5-chloro-2-formylstyryl)phenyl)carbamate 
• 1621669-63-3 C₅₂H₂₇ClN₂ 
• 1621669-64-4 C₅₂H₂₇ClN₂ 
• 1621669-56-4 C₅₂H₂₆N₂ 
• 1621669-57-5 C₅₂H₂₆N₂ 

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