60186-33-6

Usage

Uses

Used in Pharmaceutical Industry:
4-BENZYLOXY-3-ETHOXYBENZALDEHYDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 4-BENZYLOXY-3-ETHOXYBENZALDEHYDE is employed as a versatile building block for creating complex organic molecules, leveraging its aromatic properties and reactive aldehyde group.
Used in the Preparation of Heterocyclic Compounds:
4-BENZYLOXY-3-ETHOXYBENZALDEHYDE is utilized in the preparation of biologically active heterocyclic compounds, which are essential in pharmaceutical research for their potential to yield new therapeutic agents.

InChI:InChI=1/C16H16O3/c1-2-18-16-10-14(11-17)8-9-15(16)19-12-13-6-4-3-5-7-13/h3-11H,2,12H2,1H3

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 75-03-6 ethyl iodide 
• 100-44-7 benzyl chloride 

Downstream Products

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 186895-22-7 (E)-ethyl 3-{3-ethoxy-4-(benzyloxy)phenyl}acrylate 
• 55149-80-9 4-benzyloxy-5-ethoxy-2-nitro-benzaIdehyde 
• 871345-42-5 (4-benzyloxy-3-ethoxy-phenyl)-[4-(N-hydroxycarbamimidoyl)-phenylamino]-acetic acid methyl ester 

Relevant academic research and scientific papers

Alkaloids from Oxytropis ochrocephala and antiproliferative activity of sophoridine derivatives against cancer cell lines

Ten alkaloids (1-10), with sophoridine (1) as the most abundant component, were obtained from the whole plants of Oxytropis ochrocephala Bunge. Furthermore, eight new sophoridine derivatives (11-16, 20, 21), with modification on the C-14 position of 1 wer

NEW PHARMACEUTICAL COMPOUNDS

Compounds of formula (I), wherein R1-R4, X, Y and Z are as defined in claims, exhibit COMT enzyme inhibiting activity and are thus useful as COMT inhibitors.

AMIDES AND METHOD FOR PLANT DISEASE CONTROL WITH THE SAME

N-(α-cyanobenzyl)amide compounds represented by the formula (1): wherein R1 represents a hydrogen atom; a halogen atom; a C1-C6 alkyl group optionally substituted with a halogen atom or the like; or the like, R2 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group or the like, R3 represents a hydrogen atom or the like, R4 represents a C1-C4 alkyl group, a C3-C4 alkenyl group or the like, R5 represents a C1-C4 alkyl group, a C3-C4 alkenyl group, or the like, R6 represents a hydrogen atom or the like, R7 represents a hydrogen atom or the like, R8 represents a hydrogen atom or the like, R9 represents a hydrogen atom or the like, R10 represents a hydrogen atom or the like, R11 represents a hydrogen atom or the like, and R12 represents a hydrogen atom or the like, have excellent control activities against plant diseases.

AMIDE COMPOUND AND METHOD OF CONTROLLING PLANT DISEASE WITH THE SAME

A amid compound of the formula (1): wherein, in the formula, R51 represents a halogen atom, a C1-C6 alkyl group and the like; R52 represents a hydrogen atom, a halogen atom, a C1-C6 alkyl group and the like; R53 represents a halogen atom and the like; R56 represents a halogen atom and the like; R57 represents a hydrogen atom and the like; R58 and R59 independently represent a hydrogen atom, a C1-C3 alkyl group and the like; R60 represents a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C4 alkenyl group, or a C3-C6 alkynyl group; R61 represents a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C3-C4 alkenyl group or a C3-C6 alkynyl group or a C2-C4 cyanoalkyl group; R62, R63 and R64 represent a hydrogen atom, a halogen atom and the like; X represents a oxygen atom or a sulfur atom; has an excellent activity against plant diseases.