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

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

Uses

Used in Pharmaceutical Synthesis:
Methyl 2-amino-3,5-dibromobenzoate is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with enhanced properties and therapeutic effects.
Used in Organic Material Production:
Methyl 2-amino-3,5-dibromobenzoate also serves as a building block in the creation of various organic materials, contributing to the advancement of different industries that rely on organic chemistry for their products.
Used in Medicinal Chemistry Research:
Methyl 2-amino-3,5-dibromobenzoate is employed as a research tool in medicinal chemistry, aiding scientists in understanding the interactions between chemical compounds and biological targets, which is crucial for drug discovery and development.
Used in Drug Discovery:
Due to its ability to modify enzyme and receptor activities, Methyl 2-amino-3,5-dibromobenzoate is used in drug discovery processes to identify potential therapeutic agents that can treat various diseases and conditions.

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

Upstream product

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

Downstream Products

• 618-58-6 3,5-dibromobenzoic acid 
• 27003-05-0 3,5-dibromo-2-chloro-benzoic acid 
• 1049106-45-7 3,5-dibromo-2-methylamino-benzoic acid methyl ester 
• 708271-50-5 3,5-dibromo-2-methylamino-benzaldehyde 
• 51329-15-8 methyl 3,5-dibromobenzoate 
• 439940-37-1 3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-benzaldehyde 
• 439940-36-0 {3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-phenyl}-methanol 
• 439940-38-2 1,3-Bis-[(E)-2-(4-tert-butyl-phenyl)-vinyl]-5-vinyl-benzene 
• 439940-35-9 3,5-bis-[2-(4-tert-butyl-phenyl)-vinyl]-benzoic acid methyl ester 
• 76928-37-5 6,8-dibromo-1H-benzo[d][1,3]oxazin-2(4H)-one 
• 50739-76-9 (2-amino-3,5-dibromophenyl)methanol 

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;

1-CYANO-PYRROLIDINE DERIVATIVES AS DUB INHIBITORS

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30). The novel compounds have formula (I): (Formula (I)) or are pharmaceutically acceptable salts thereof, wherein: R1a, R1b, R1c, R1d, R1e and R1f each independently represent hydrogen, optionally substituted C1-C6 alkyl or optionally substituted C3-C4 cycloalkyl, or R1b and R1c together form an optionally substituted C3-C6 cycloalkyl ring, or R1d and R1e together form an optionally substituted C3-C6 cycloalkyl ring; R2 represents hydrogen or optionally substituted C1-C6 alkyl; A represents an optionally further substituted 5 to 10 membered monocyclic or bicyclic heteroaryl, heterocyclyl or aryl ring; L represents a covalent bond or linker; B represents an optionally substituted 3 to 10 membered monocyclic or bicyclic heterocyclyl, heteroaryl, cycloalkyl or aryl ring; and when -A-L-B is at position x attachment to A is via a carbon ring atom of A, and either: A cannot be triazolopyridazinyl, triazolopyridinyl, imidazotriazinyl, imidazopyrazinyl or pyrrolopyrimidinyl; or B cannot be substituted with phenoxyl; or B cannot be cyclopentyl when L is an oxygen atom.

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

Cu-mediated selective bromination of aniline derivatives and preliminary mechanism study

A simple and efficient bromination of aniline, aniline derivatives, and analogs have been developed. Forty three examples were given and the highest yield reached was 98%. Different substrates including substituted aniline, pyridin-amine, N-substituted aniline, N,N-disubstituted aniline, N-phenyl-amide, N-phenyl-sulfonamide, and nitrogen-containing heterocycles were all reactive and selectively generated desired bromo-products. The method can be applied to synthesize drug intermediate and quinoxaline derivatives.

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.

Discovery of 3-aryl-3-methyl-1H-quinoline-2,4-diones as a new class of selective 5-HT6 receptor antagonists

A 5,7-dichloro-3-phenyl-3-methyl-quinoline-2,4-dione (11a) has been identified in a random screen as a lead for 5-HT6 antagonist. During the lead optimization process, several analogs were synthesized and their biological activities were investigated. Within this series, several compounds display high binding affinity and selectivity for the 5-HT6 receptor. In particular, 3-(4-hydroxyphenyl)-3-methyl-quinoline-2,4-dione (12f) exhibits high affinity (Ki = 12.3 nM) for 5-HT6 receptor with good selectivity over other serotonin and dopamine (D1-D4) receptor subtypes. In a functional adenylyl cyclase stimulation assay, this compound exhibited considerable antagonistic activity (IC50 = 0.61 μM).

Synthesis of dendritic stilbenoid compounds: Heck reactions for the periphery and the core

A convergent synthetic strategy for stilbenoid dendrimers is described in which multifold Heck reactions have been used to construct both the peripheral and the core stilbene units. Solution optical properties of one of the dendrimers indicated some energy transfer having taken place from the periphery to the core.

Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate

The selective monobromination of various deactivated anilines using potassium bromide and sodium perborate as oxidant has been achieved. The use of ammonium molybdate as catalyst accelerates the rate of reaction but is not essential to obtain good yields and high selectivities. (C) 2000 Elsevier Science Ltd.

Chiroptical Detection During Liquid Chromatography, Part 5: On-Line Measurement of Circular Dichroism Spectra Δε(λ) During Stops of Chromatographic Flow

A procedure is described which serves to measure circular dichrograms Δε(λ) on line during stops of flow in liquid chromatography.Since the concentration of substrate in the spectrometer cell during the stop is not known, the differential absorption coeff

Process for the selective reduction of the 4-halogen in 2,4-dihaloanilines

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