58026-13-4

Basic information

• Product Name: 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene
• Synonyms: 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene
• CAS NO: 58026-13-4
• Molecular Weight: 307.187
• Mol File: 58026-13-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene(58026-13-4)
• EPA Substance Registry System: 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene(58026-13-4)

Safety Data

• Hazardous Substances Data: 58026-13-4(Hazardous Substances Data)

Upstream product

• 54915-31-0 methyl 3-(benzyloxy)-5-hydroxybenzoate 
• 19520-74-2 3-hydroxy-5-methoxy-benzoic acid methyl ester 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 50637-26-8 methyl 3-(benzyloxy)-5-methoxybenzoate 
• 50637-28-0 (3-(benzyloxy)-5-methoxyphenyl)methanol 

Downstream Products

• 1437308-45-6 methyl 5-(3-benzyloxy-5-methoxyphenyl)-4-methyl-3-oxopentanoate 
• 1437308-53-6 methyl 8-benzyloxy-2-hydroxy-6-methoxy-3-methylnaphthalene-1-carboxylate 
• 60347-67-3 3-[2-(2-hydroxyphenyl)ethyl]-5-methoxyphenol 
• 56684-87-8 batatasin-III 
• 1187459-67-1 Br^(1-)*C₂₁H₃₀NO₂⁽¹⁺⁾ 
• 83088-11-3 3',5-dibenzyloxy-3,4'-dimethoxy-2'-(3-methylbut-2-enyl)stilbene 
• 71135-76-7 cis-trans-3',5-dibenzyloxy-3,4'-dimethoxystilbene 
• 83088-27-1 C₃₀H₂₈O₄ 
• 42438-89-1 3,4'-dihydroxy-5-methoxystilbene 
• 83088-28-2 gigantol 
• 70677-47-3 canniprene 
• 67884-30-4 5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxyphenol 
• 67884-29-1 3,4'-dihydroxy-5-methoxybibenzyl 
• 54922-80-4 (3-(benzyloxy)-5-methoxybenzyl)triphenylphosphonium bromide 

Relevant articles and documents

PHENANTHRENE AMPK ACTIVATOR COMPOUNDS, COMPOSITIONS, METHODS AND USES THEREOF

The present invention relates to a compound having general formula I for use in the activation of AMPK. A composition comprising said compound for use in the activation of AMPK is also provided.

Naturally occurring Batatasins and their derivatives as α-glucosidase inhibitors

Batatasins are endogenous plant hormones found in yams and other related plant species. These plants are widely consumed as botanical dietary supplements in many parts of the world. This study investigated the inhibitory effects and mechanisms of Batatasin I, III, IV, V against α-glucosidase regarding their antidiabetic activities. The results revealed that Batatasin I, III, IV inhibited α-glucosidase in a reversible and noncompetitive manner, with IC50 values of 2.55, 1.89 and 2.52 mM respectively, while Batatasin V completely abolished its inhibitory activity even at the highest concentrations tested. Furthermore, a class of Batatasin-derived compounds with different substitution patterns was synthesized and subjected to the assay to clarify the structure-activity relationships, which suggested that the hydroxyl at the C-2′ position may play a significant role in improving the inhibitory activities. Their probable binding modes and the specificity of the binding sites were studied using molecule docking simulation. It was concluded that Batatasins, especially Batatasin III and IV, are promising α-glucosidase inhibitors, which therefore could be used as functional food to alleviate postprandial hyperglycemia and as potential candidates for the development of antidiabetic agents.

Dendrimer disassembly in the gas phase: A cascade fragmentation reaction of frechet dendrons

The mass spectrometry characterization of Frechet-type dendrons is reported. In order to provide the charges necessary for electrospray ionization, dendrons bearing an OH group at the focal point can be deprotonated and observed in the negative ion mode.