152626-77-2

Basic information

• Product Name: 5-AMINO-2-BROMO-4-METHYLANISOLE
• Synonyms: 5-AMINO-2-BROMO-4-METHYLANISOLE;4-broMo-5-Methoxy-2-Methylaniline;4-BroMo-5-Methoxy-2-Methyl-phenylaMine
• CAS NO: 152626-77-2
• Molecular Formula: C₈H₁₀BrNO
• Molecular Weight: 216.08
• Mol File: 152626-77-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 79-80 °C
• Boiling Point: 288.4±35.0 °C(Predicted)
• Appearance: /
• Density: 1.458±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 3.32±0.10(Predicted)
• CAS DataBase Reference: 5-AMINO-2-BROMO-4-METHYLANISOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-AMINO-2-BROMO-4-METHYLANISOLE(152626-77-2)
• EPA Substance Registry System: 5-AMINO-2-BROMO-4-METHYLANISOLE(152626-77-2)

Safety Data

• Hazardous Substances Data: 152626-77-2(Hazardous Substances Data)

Usage

General Description

5-Amino-2-bromo-4-methylanisole is a chemical compound that belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. It has a molecular formula of C8H10BrNO and molecular weight of 216.08 g/mol. Generally, anisoles are aromatic chemical compounds that have substitution of a hydroxy group by a methoxy group and similar structures with methane substructures. There is limited information available about its specific uses; it may be used in the manufacture of other chemicals or in laboratory research. Few studies have been conducted on this chemical to assess its toxicity or environmental effects.

Upstream product

• 50868-72-9 5-methoxy-o-toluidine 
• 134-19-0 2-methoxy-4-nitro-5-methyl aniline 
• 50868-75-2 5’-methoxy-2’-methylacetanilide 
• 871878-59-0 acetic acid-(4-bromo-5-methoxy-2-methyl-anilide) 

Downstream Products

• 1613504-76-9 4-bromo-5-methoxy-2-methylbenzenediazonium tetrafluoroborate 
• 1613505-30-8 6-cyclopropyl-1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 1613505-29-5 1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazol-6-yl trifluoromethanesulfonate 
• 1613505-28-4 1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazol-6-ol 
• 1613505-15-9 6-methoxy-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 1613505-31-9 6-cyclopropyl-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 152626-78-3 5-bromo-6-methoxy-1H-indazole 
• 1613504-91-8 C₂₀H₁₉F₃N₂O₂ 

Relevant articles and documents

NEW COMPOUND AND USE THEREOF

PROBLEM TO BE SOLVED: To provide a compound for visualizing TRPA1 in an organism. SOLUTION: The invention provides a compound represented by the formula (1) or (2) in the figure or a salt thereof. (In the formulas, R1 and R2 are each a substituent having a radioisotope.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

FUNGICIDAL COMPOSITIONS

A fungicidal composition comprising a mixture of a N-phenylamidine defined by formula (I) as component (A) and a further pesticide as component (B) as defined in claim 1, as well as the use of the composition in agriculture or horticulture for controlling or preventing infestation of plants by phytopathogenic microorganisms, preferably fungi.

Synthesis and reactivity of dimethoxy-functionalised Troeger's base analogues

Troeger's base analogues were prepared bearing methoxy groups in the 1,7-, 2,8-, 3,9- or 4,10-positions. These compounds were converted to their dihydroxy analogues in excellent yields upon treatment with boron tribromide and the 4,10-dihydroxy analogue could be prepared by directly from 4-hydroxyaniline. The synthetic utility of the dihydroxy-functionalised compounds as building blocks was demonstrated by the synthesis of a dialkoxy and a diester Troeger's base analogue.