606-00-8

Basic information

• Product Name: Methyl 2-amino-3,5-dibromobenzoate
• Synonyms: METHYL 3,5-DIBROMOANTHRANILATE;METHYL 2-AMINO-3,5-DIBROMOBENZOATE;3,5-DIBROMOANTHRANILIC ACID METHYL ESTER;2-AMINO-3,5-DIBROMOBENZOIC ACID METHYL ESTER;2-Amino-3,5-dibromobenzoic acid methyl ester~Methyl 3,5-dibromoanthranilate;Mehtyl 3,5-Dibromoanthranilate;2-amino-3,5-dibromo benzate ester;METHYL 3,5-DIBROMOANTHRANULATE
• CAS NO: 606-00-8
• Molecular Formula: C₈H₇Br₂NO₂
• Molecular Weight: 308.95
• EINECS: 400-990-8
• Product Categories: Organic acids;Acids & Esters;Anilines, Amides & Amines;Bromine Compounds
• Mol File: 606-00-8.mol
• Article Data: 10

Chemical Properties

• Melting Point: 89-91 °C(lit.)
• Boiling Point: 317.9 °C at 760 mmHg
• Flash Point: 146.1 °C
• Appearance: /
• Density: 1.907 g/cm³
• Vapor Pressure: 0.000373mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: -0.30±0.10(Predicted)
• BRN: 3257505
• CAS DataBase Reference: Methyl 2-amino-3,5-dibromobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-amino-3,5-dibromobenzoate(606-00-8)
• EPA Substance Registry System: Methyl 2-amino-3,5-dibromobenzoate(606-00-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 606-00-8(Hazardous Substances Data)

Usage

General Description

Methyl 2-amino-3,5-dibromobenzoate is a chemical compound with the molecular formula C9H8Br2NO2. It is a derivative of benzoic acid and contains two bromine atoms and an amino group. Methyl 2-amino-3,5-dibromobenzoate is commonly used in the synthesis of pharmaceutical compounds and organic materials. It has been found to have potential applications in medicinal chemistry and drug discovery due to its ability to modify the activity of enzymes and receptors in the body. Methyl 2-amino-3,5-dibromobenzoate is a valuable building block for the production of various pharmaceuticals and other organic compounds.

InChI:InChI=1/C8H7Br2NO2/c1-13-8(12)5-2-4(9)3-6(10)7(5)11/h2-3H,11H2,1H3

Upstream product

• 77-78-1 dimethyl sulfate 
• 609-85-8 2-amino-3,5-dibromobenzoic acid 
• 186581-53-3 diazomethane 
• 134-20-3 2-carbomethoxyaniline 
• 52727-57-8 5-bromo-2-aminobenzoic acid methyl ester 

Downstream Products

• 16524-04-2 2‐amino‐3,5‐dibromobenzamide 
• 50739-76-9 (2-amino-3,5-dibromophenyl)methanol 
• 76928-37-5 6,8-dibromo-1H-benzo[d][1,3]oxazin-2(4H)-one 
• 439940-35-9 3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-benzoic acid methyl ester 
• 439940-38-2 1,3-Bis-[(E)-2-(4-tert-butyl-phenyl)-vinyl]-5-vinyl-benzene 
• 439940-36-0 {3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-phenyl}-methanol 
• 439940-37-1 3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-benzaldehyde 
• 51329-15-8 methyl 3,5-dibromobenzoate 
• 708271-50-5 3,5-dibromo-2-methylamino-benzaldehyde 

Relevant articles and documents

Synthesis process of ambroxol hydrochloride

The invention relates to a synthesis process of ambroxol hydrochloride. The method comprises the following steps: carrying out bromination reaction on methyl anthranilate under the action of molecularbromine and hydrogen peroxide to generate a compound 3;

A preparation method of bromhexine hydrochloride (by machine translation)

The invention belongs to the field of organic synthesis, provides a bromhexine hydrochloride of the preparation method. The invention relates to 2 - aminobenzoic acid ester compound as a raw material, by the bromo reaction, reduction reaction, condensatio

Design, synthesis and optical response of pyridine-cored V-shaped stilbenoid dendrimers

Design, synthesis and characterization of new series of first-generation V-shaped dendrimers bearing phenylenevinylene dendritic branches in periphery and pyridine as a core is described. A preliminary study of the optical properties of the resulting compounds was conducted by UV/vis and fluorescence spectroscopy.