1486-52-8

Basic information

• Product Name: Benzoyl chloride, 3-methoxy-4-(phenylmethoxy)-
• CAS NO: 1486-52-8
• Molecular Formula: C15H13ClO3
• Molecular Weight: 276.719
• Mol File: 1486-52-8.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 3-methoxy-4-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3-methoxy-4-(phenylmethoxy)-(1486-52-8)
• EPA Substance Registry System: Benzoyl chloride, 3-methoxy-4-(phenylmethoxy)-(1486-52-8)

Safety Data

• Hazardous Substances Data: 1486-52-8(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 100-39-0 benzyl bromide 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 91203-74-6 4-benzyloxy-3-methoxybenzoic acid benzyl ester 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 185033-64-1 ethyl 4-benzyloxy-3-methoxybenzoate 
• 617-05-0 ethyl vanillate 
• 1486-53-9 4-(benzyloxy)-3-methoxybenzoic acid 

Downstream Products

• 81581-25-1 ethyl 2-(4-benzyloxy-3-methoxybenzoyl)acetoacetate 
• 1592-47-8 4-(benzyloxy)-3-methoxybenzoic anhydride 
• 66832-24-4 2-<(trichloromethyl)thio>pyridine 
• 63057-72-7 2-benzyloxy-5-bromoanisole 
• 89456-24-6 4-Benzyloxy-3-methoxy-benzoic acid 2-acetyl-6-benzyloxy-3,5-dimethoxy-phenyl ester 
• 857598-54-0 4-benzyloxy-3-methoxy-benzoic acid-(2-benzo[1,3]dioxol-5-yl-2-methoxy-1-methyl-ethylamide) 
• 855946-93-9 4-benzyloxy-3-methoxy-benzoic acid-(4-hydroxy-3-methoxy-phenethylamide) 
• 148235-48-7 4-benzyloxy-3-methoxy-benzoic acid-(4-benzyloxy-3-methoxy-phenethylamide) 
• 926026-35-9 tert-butyl {2-[(4-benzyloxy-3-methoxybenzoyl)(2-thienylmethyl)amino]ethyl}carbamate 
• 38209-42-6 threo-2,3-bis-(α-hydroxy-4-hydroxy-3-methoxybenzyl)butane-1,4-diol 
• 854847-71-5 5-(4-benzyloxy-3-methoxy-phenyl)-7-methyl-[1,3]dioxolo[4,5-g]isoquinoline 
• 855647-29-9 7-benzyloxy-1-(4-benzyloxy-3-methoxy-phenyl)-6-methoxy-3,4-dihydro-isoquinoline 

Relevant articles and documents

Synthesis and antitumor activity of novel pyridoxine-based structural analogs of saccharumoside-B

A series of 11 new pyridoxine-based structural analogs of saccharumoside-B were obtained using original synthetic approach. Antitumor activity of these compounds against nine human tumor cell lines (MCF-7, MDA-MB-231, A-498, SNB-19, M-14, NCI-H322M, HCT-115, HCT-116, and PC-3) was studied, and cytotoxic activity to three normal (HEK-293, Chang Liver, and MSC) cell lines was evaluated. Among the synthesized compounds, 12d, 12e, 13b, 13d, 13e, and 14 exhibited the highest antitumor activity, comparable to that of camptothecin and doxorubicin, but with significantly increased selectivity toward tumor cells. [Figure not available: see fulltext.]

AMINATED LIGNIN-DERIVED COMPOUNDS AND USES THEREOF

The present invention relates to novel lignin-derived compounds and compositions comprising the same and their use as redox flow battery electrolytes. The invention further provides a method for preparing said compounds and compositions as well as a redox flow battery comprising said compounds and compositions. Additionally, an assembly for carrying out the inventive method is provided.

An alternate method for the synthesis of 2-aryl/alkyl-5-bromo-7-methoxy benzofurans; application to the synthesis of Egonol, Homoegonol, and analogs via Heck reaction

We herein report the general, versatile, and convenient method for the synthesis of 2-arly/alkyl-5-bromo-7-methoxy benzofurans from easily available o-Vanillin in five steps. These benzofurans was successfully converted into biological active natural products Egonol, Homoegonol, and analogous on applying Heck reaction using ethyl/methyl acrylate in the presence of palladium catalyst.