59557-92-5

Basic information

• Product Name: 2-BROMO-5-METHOXYANILINE
• Synonyms: 2-BROMO-5-METHOXYANILINE;4-Bromo-3-amino anisole;2-bromo-5-methoxybenzenamine;2-Bromo-5-Methoxyaniline (In HCl salt form);2-BROMO-5-METHOXYANI;2-BroMo-5-Methoxy-phenylaMine;2-Bromo-5-methoxyaniline 97%;3-Amino-4-bromoanisole, 6-Bromo-m-anisidine
• CAS NO: 59557-92-5
• Molecular Formula: C₇H₈BrNO
• Molecular Weight: 238.51
• EINECS: 1312995-182-4
• Product Categories: Amines;Phenyls & Phenyl-Het;Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;Phenyls & Phenyl-Het
• Mol File: 59557-92-5.mol
• Article Data: 33

Chemical Properties

• Melting Point: 189-190°C
• Boiling Point: 280.055 °C at 760 mmHg
• Flash Point: 123.173 °C
• Appearance: /
• Density: 1.532g/cm³
• Vapor Pressure: 0.004mmHg at 25°C
• Refractive Index: 1.596
• Storage Temp.: Room temperature.
• PKA: 2.11±0.10(Predicted)
• CAS DataBase Reference: 2-BROMO-5-METHOXYANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-5-METHOXYANILINE(59557-92-5)
• EPA Substance Registry System: 2-BROMO-5-METHOXYANILINE(59557-92-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 59557-92-5(Hazardous Substances Data)

Usage

General Description

2-BROMO-5-METHOXYANILINE, also known as 5-Bromo-2-methoxyaniline, is a chemical compound with the molecular formula C7H8BrNO. It is a bromo-substituted aniline derivative that is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. The presence of a bromine and a methoxy group in the molecule makes it a versatile building block for the synthesis of various biologically active compounds. It is also used in the production of agrochemicals and fine chemicals. Additionally, 2-BROMO-5-METHOXYANILINE has applications in the field of materials science, particularly in the development of polymers and functional materials. However, it is important to handle this chemical with care as it can be hazardous if mishandled or improperly stored.

InChI:InChI=1/C7H8BrNO/c1-10-5-2-3-6(8)7(9)4-5/h2-4H,9H2,1H3

Upstream product

• 51-66-1 4-methoxyacetanilide 
• 5344-78-5 4-bromo-3-nitroanizole 
• 577-72-0 4-methoxy-3-nitroaniline 
• 536-90-3 m-Anisidine 
• 7439-89-6 iron 
• 7646-78-8 tin(IV) chloride 
• 119-81-3 4-methoxy-2-nitroacetanilide 
• 96-96-8 4-methoxy-2-nitroaniline 
• 110-00-9 furan 

Downstream Products

• 138642-47-4 2-bromo-5-methoxybenzonitrile 
• 3189-13-7 6-methoxylindole 
• 86045-69-4 4-methoxy-2-(trimethylacetamido)benzaldehyde 
• 887469-87-6 4-bromo-3-methoxycarbamoylanisole 
• 643069-37-8 5-[(2-bromo-5-methoxy-phenylamino)-methylene]-2,2-dimethyl-[1,3]dioxane-4,6-dione 
• 438248-63-6 4-(2-Bromo-5-methoxyanilino)-2-(3-pyridinyl)-6-(trifluoromethyl)pyrimidine 
• 81224-16-0 7-bromo-4-methoxy-1H-indole 
• 1402939-10-9 (Z)-methyl N-2-bromo-5-methoxyphenylbenzimidate 
• 1402939-24-5 7-methoxy-2-phenyl-3-p-tolylquinazolin-4(3H)-one 
• 1027340-49-3 5-methoxy-2-((trimethylsilyl)ethynyl)aniline 
• 123027-99-6 N-(2-bromo-5-methoxyphenyl)ethanamide 

Relevant articles and documents

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

This disclosure relates to compounds having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such compounds and intermediates used in such processes, compositions containing such compounds, and processes of using such compounds against such pests. These compounds/molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses compounds having the following formula (Formula One and/or Formula One-A).

Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts

The enantioselective syntheses of axially chiral heterobiaryls were accomplished through the aromatic electrophilic halogenation of 3-(quinolin-8-yl)phenols with bifunctional organocatalysts that control the molecular conformations during successive halogenations. Axially chiral quinoline derivatives, which have rarely been synthesized in an enantioselective catalytic manner, were afforded in moderate-to-good enantioselectivities through bromination, and an analogous protocol also enabled enantioselective iodination. In addition, this catalytic reaction, which allows enantioselective control through the use of mono-ortho-substituted substrates, allowed the asymmetric synthesis of 8-arylquinoline derivatives bearing two different halogen groups in high enantioselectivities.

Homogenous suspension of immunopotentiating compounds and uses thereof

The present invention generally relates to homogeneous suspensions of small molecule immune potentiators (SMIPs) that are capable of stimulating or modulating an immune response in a subject in need thereof. The homogeneous suspensions may be used in combinations with various antigens or adjuvants for vaccine therapies.