138505-27-8

Usage

Uses

Used in Organic Synthesis:
4-bromo-1-isopropoxy-2-methoxybenzene is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure allows for the formation of complex organic molecules that can be utilized in the development of new drugs and agricultural products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-bromo-1-isopropoxy-2-methoxybenzene serves as a key intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can influence the biological activity and pharmacological properties of the final product, making it a valuable component in drug discovery and development.
Used in Perfume and Fragrance Manufacturing:
4-bromo-1-isopropoxy-2-methoxybenzene is used as a raw material in the manufacturing of perfumes and fragrances due to its strong aromatic odor. Its unique scent profile can be incorporated into various fragrance formulations, contributing to the overall olfactory experience of the final product.
Used in Materials Science:
4-bromo-1-isopropoxy-2-methoxybenzene has potential applications in the field of materials science, where it can be used to develop new materials with specific properties. Its chemical structure may contribute to the creation of materials with unique characteristics, such as improved stability, reactivity, or other desirable traits.
Used as a Chemical Intermediate in Various Industries:
In addition to its direct applications, 4-bromo-1-isopropoxy-2-methoxybenzene also serves as a chemical intermediate in various industries. Its versatility allows it to be used in the production of a wide range of products, from specialty chemicals to advanced materials, making it a valuable component in the chemical manufacturing process.

Upstream product

• 67-63-0 isopropyl alcohol 
• 103291-07-2 4-bromo-1-fluoro-2-methoxy-benzene 
• 1761-61-1 5-bromosalicyclaldehyde 
• 138505-25-6 2-(2-propoxy)-5-bromobenzaldehyde 
• 90-05-1 2-methoxy-phenol 
• 7368-78-7 4-bromoguaiacol 
• 75-26-3 isopropyl bromide 
• 138505-26-7 5-Bromo-2-isopropoxyphenol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 7368-78-7 4-bromoguaiacol 
• 875654-33-4 4-isopropoxy-3-methoxyphenylboronic acid 
• 133593-77-8 4,5-Dihydro-2-<1-(4-isopropoxy-3-methoxyphenyl)-5,7-diisopropoxy-2-naphthyl>-4,4-dimethyloxazole 
• 133773-24-7 1-(4-Isopropoxy-3-methoxyphenyl)-3-(4-isopropoxy-3-methoxybenzyl)-5,7-diisopropoxy-2-methylnaphthalene 
• 133593-79-0 [3-Hydroxymethyl-6,8-diisopropoxy-4-(4-isopropoxy-3-methoxy-phenyl)-naphthalen-2-yl]-(4-isopropoxy-3-methoxy-phenyl)-methanol 
• 133593-78-9 (+/-)-3,9-Bis(4-isopropoxy-3-methoxyphenyl)-5,7-diisopropoxynaphtho<2,3-c>furan-1(3H)-one 
• 138505-24-5 (+/-)-1,3-Dihydro-3,9-bis(4-isopropoxy-3-methoxyphenyl)-5,7-diisopropoxynaphtho<2,3-c>furan 
• 660396-67-8 3,11-diisopropoxy-14-(4-isopropoxy-3-methoxyphenyl)-2,12-dimethoxy-6H-chromeno[4′,3′:4,5]pyrrolo[2,1-a]-isoquinolin-6-one 
• 97614-65-8 lamellarin D 
• 875654-41-4 methyl 3,4-dihydro-7-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrole-2-carboxylate 
• 875654-43-6 3,4-dihydro-7-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrole-2-carboxylic acid 
• 660396-69-0 5,6-dihydro-3,11-diisopropoxy-14-(4-isopropoxy-3-methoxyphenyl)-2,12-dimethoxy-6H-[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one 
• 875654-39-0 dimethyl 3-(4-isopropoxy-3-methoxyphenyl)-1-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-4-(trifluoromethanesulfonyloxy)pyrrole-2,5-dicarboxylate 
• 875654-30-1 7-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)ethyl]-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrol-4(3H)-one 

Relevant academic research and scientific papers

Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids

Pyruvic acid and other α-keto acids are frequently encountered as intermediates in metabolic pathways, yet their application in total synthesis has met with limited success. In this work, we present a bioinspired strategy that utilizes highly functionaliz

PYRAN-SPIROCYCLIC PIPERIDINE AMIDES AS MODULATORS OF ION CHANNELS

The invention relates to pyran spirocyclic piperidine amide compounds useful as inhibitors of ion channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the composition

Short synthesis and antimalarial activity of fagaronine

Herein, we report a new synthesis of fagaronine 1, inspired by the synthesis reported by Luo for nornitidine. The in vitro biological activity of fagaronine against malaria on several chloroquine-sensitive and resistant Plasmodium falciparum strains was c

Total synthesis of lamellarins D, L, and N

Total synthesis of cytotoxic marine alkaloids, lamellarins D, L, and N, has been achieved by using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki-Miyaura coupling of the 3,4-dihydroxypyrrole bistriflate 6 as the key reactions. The total yields of lamellarins D, L, and N from the common intermediate 6 are 54, 58, and 50%, respectively.

Synthesis of Larreantin, a Cytotoxic Napththoquinoid Sesquilignan from Larrea tridentata

Larreantin 1, a biogenetically unique cytotoxic naphthoquinoid sesquilignan has been synthesized by a convergent route.The key intermediate was 4,5-dihy