365572-23-2

Basic information

• Product Name: 2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol
• Synonyms: 2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol
• CAS NO: 365572-23-2
• Molecular Weight: 289.169
• Mol File: 365572-23-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol(365572-23-2)
• EPA Substance Registry System: 2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol(365572-23-2)

Safety Data

• Hazardous Substances Data: 365572-23-2(Hazardous Substances Data)

Upstream product

• 1016650-10-4 2-(3-isopropoxy-4-methoxyphenyl)ethanol 
• 56517-32-9 2-bromo-4-methoxy-5-(1-methylethoxy)benzaldehyde 
• 867313-46-0 2-bromo-5-isopropoxy-4-methoxystyrene 
• 365572-22-1 2-bromo-4-methoxy-5-(1-methylethoxy)benzeneacetaldehyde 

Downstream Products

• 1016650-11-5 2-(2-bromo-5-isopropoxy-4-methoxyphenethoxy)triisopropylsilane 
• 1192217-73-4 3-[2-(2-bromo-5-isopropoxy-4-methoxyphenyl)ethyl]-7-isopropoxy-8-methoxy[1]benzopyrano[3,4-b]pyrrol-4(3H)-one 
• 365572-26-5 2-[2-[2-bromo-4-methoxy-5-(1-methylethoxy)phenyl]ethyl]-2-[4-(1-methylethoxy)phenylmethyl]propane-1,3-dicarboxylic acid dimethyl ester 
• 365572-27-6 4-(2-bromo-5-isopropoxy-4-methoxy-phenyl)-2-(4-isopropoxy-benzyl)-butyric acid 
• 365572-28-7 4-(2-bromo-5-isopropoxy-4-methoxy-phenyl)-2-(4-isopropoxy-benzyl)-butyramide 
• 365572-29-8 4-(2-bromo-5-hydroxy-4-methoxy-phenyl)-2-(4-hydroxy-benzyl)-butyramide 
• 365572-25-4 2-[2-[2-bromo-4-methoxy-5-(1-methylethoxy)phenyl]ethyl]propane-1,3-dicarboxylic acid dimethyl ester 
• 897017-95-7 1,2-bis-(4-hydroxy-3-methoxy-phenyl)-8-isopropoxy-9-methoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-3-carboxylic acid methyl ester 
• 850346-69-9 2-(2-bromo-5-isopropoxy-4-methoxyphenyl)ethyl p-toluenesulfonate 
• 365572-24-3 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene 
• 97614-65-8 lamellarin D 
• 867313-42-6 methyl 2-(2,4-diisopropoxy-5-methoxyphenyl)-8-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-9-methoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate 
• 867313-43-7 methyl 2-(2,4-diisopropoxy-5-methoxyphenyl)-8-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-9-methoxypyrrolo[2,1-a]isoquinoline-3-carboxylate 
• 867313-44-8 methyl 2-(2,4-dihydroxy-5-methoxyphenyl)-8-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-9-methoxypyrrolo[2,1-a]isoquinoline-3-carboxylate 

Relevant articles and documents

Design and synthesis of lamellarin D analogues targeting topoisomerase I

(Chemical Equation Presented) A general synthetic route to rationally designed lamellarinDanalogues, 1-dearyllamellarinD(1) and 1-substituted 1-dearyllamellarin D (2), has been developed. The key pentacyclic intermediate 22 was prepared by palladium-catalyzed direct arylation of 12, which in turn was synthesized via C-2-selective lithiation of 15 followed by palladium-catalyzed cross-coupling as the key reactions. Compound 22 was converted to a wide range of C-1-substituted analogues 2 via regioselective electrophilic substitution and palladium-catalyzed cross-coupling reactions.

Di- and triarylsubstituted pyrroles by sequential regioselective cross-coupling reactions

The di- and tribrominated pyrroles, such as methyl 3,4,5-tribromo- pyrrole-2-carboxylate (1), ethyl 3,4,5-tribromopyrrole-2-carboxylate (2), methyl 4,5-dibromopyrrole-2-carboxylate (3), and 4,5-dibromo-2-nitropyrrole (4), were prepared and evaluated for t

5,6-Dihydropyrrolo[2,1-b]isoquinolines as scaffolds for synthesis of lamellarin analogues

Efficient modular synthetic routes to open chain marine alkaloids such as lamellarins have been developed. 5,6-Dihydropyrrolo[2,1-b]isoquinoline scaffolds were prepared, and protocols enabling regioselective bromination followed by Suzuki cross-coupling were established for the introduction of aryl groups onto the 2- and 3-positions.

4a,5,9,10,11,12-hexahydro-6H-benzo[a]cyclohepta[hi]benzo-furan - Synthesis of unnatural galanthamine analogs

The synthesis of an unnatural galanthamine analog is reported.