152946-38-8

Basic information

• Product Name: 2-Amino-6-bromo-5-methoxybenzoic acid
• Synonyms: 2-Amino-6-bromo-5-methoxybenzoic acid;6-AMino-2-broMo-3-Methoxybenzoic acid
• CAS NO: 152946-38-8
• Molecular Formula: C₈H₈BrNO₃
• Molecular Weight: 246.05802
• Mol File: 152946-38-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 378.6±42.0 °C(Predicted)
• Appearance: /
• Density: 1.703±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 0.73±0.10(Predicted)
• CAS DataBase Reference: 2-Amino-6-bromo-5-methoxybenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-6-bromo-5-methoxybenzoic acid(152946-38-8)
• EPA Substance Registry System: 2-Amino-6-bromo-5-methoxybenzoic acid(152946-38-8)

Safety Data

• Hazardous Substances Data: 152946-38-8(Hazardous Substances Data)

Usage

Main properties

Chemical compound
Contains a benzene ring
Contains a 2-amino group
Has a 6-bromo substituent
Has a 5-methoxy substituent
Derivative of benzoic acid
Used in pharmaceutical and chemical industries
Potential applications in medicinal chemistry

Specific content

Building block for the synthesis of various drugs and organic compounds
Potential applications in drug discovery
Possible biological activity
Valuable chemical intermediate

Structural Features

Benzene ring with a 2-amino group
Substituent at the 6th position: Bromo (Br)
Substituent at the 5th position: Methoxy (OCH?)

Derivative of

Benzoic acid

Industries

Pharmaceutical and Chemical

Applications

Used in the synthesis of various drugs and organic compounds
Potential applications in medicinal chemistry

Role in Drug Discovery

Building block for synthesizing novel drug candidates

Potential Biological Activity

May exhibit biological activity
Subject to investigation for pharmacological effects

Value

Valuable chemical intermediate
Diverse applications in drug discovery and chemical research

Upstream product

• 19056-41-8 3-bromo-p-anisidine 
• 130420-75-6 4-bromo-5-methoxyisatin 

Relevant articles and documents

ANTIPROLIFERATIVE QUINAZOLINES

Quinazoline compounds which demonstrate antiproliferative activity, such as antitumor activity, processes of preparing these compounds, pharmaceutical compositions containing these compounds, and the use of these compounds. These compounds inhibit the growth and proliferation of the cells of higher organisms and microorganisms,such as bacteria, yeasts and fungi. Preferred quinazoline compounds are capable of inhibiting the enzyme thymidylate synthase. Effects derived from the inhibition of the enzyme thymidylate synthase include those discussed above