151541-15-0

Basic information

• Product Name: Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate
• Synonyms: Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate
• CAS NO: 151541-15-0
• Molecular Formula: C₂₇H₃₀O₈
• Molecular Weight: 482.5223
• Mol File: 151541-15-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 641.4±55.0 °C(Predicted)
• Appearance: /
• Density: 1.209±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Store in freezer, under -20°C
• PKA: 12.56±0.20(Predicted)
• CAS DataBase Reference: Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate(151541-15-0)
• EPA Substance Registry System: Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate(151541-15-0)

Safety Data

• Hazardous Substances Data: 151541-15-0(Hazardous Substances Data)

Usage

General Description

Ethyl 3-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate is a complex chemical compound with a long molecular structure. It contains an ethyl group, a phenyl group, and several hydroxy and methoxy groups. The compound also includes a propanoate moiety, which is a type of ester. This chemical may have potential pharmaceutical or industrial applications, but further research and testing would be needed to determine its specific uses. The compound's intricate structure suggests that it could have unique properties and behaviors, making it an interesting subject for study in the field of chemistry.

Upstream product

• 13078-21-2 ethyl 2-(2-methoxyphenoxy)acetate 
• 6527-32-8 4-(benzyloxy)-3,5-dimethoxybenzaldehyde 
• 90-05-1 2-methoxy-phenol 
• 100-39-0 benzyl bromide 
• 134-96-3 syringic aldehyde 
• 100-44-7 benzyl chloride 

Downstream Products

• 535967-76-1 1-(4-(benzyloxy)-3,5-dimethoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol 
• 92409-34-2 1-(4-hydroxy-3,5-dimethoxyphenyl)-2-(2'-methoxyphenoxy)-1,3-propanediol 
• 136196-47-9 3-hydroxy-1-(3,5-dimethoxy-4-hydroxyphenyl)-propan-1-one 
• 90-05-1 2-methoxy-phenol 
• 19513-80-5 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethan-1-one 
• 92409-23-9 3-hydroxy-2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)propan-1-one 
• 535967-82-9 1-(4-(benzyloxy)-3,5-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one 
• 6437-46-3 1-(2-methoxyphenoxy)propan-2-one 
• 92444-02-5 4-[(E)-3-Hydroxy-2-(2-methoxy-phenoxy)-propenyl]-2,6-dimethoxy-phenol 
• 503444-15-3 (E)-3-(4-Benzyloxy-3,5-dimethoxy-phenyl)-2-(2-methoxy-phenoxy)-acrylic acid ethyl ester 

Relevant articles and documents

Sequential Cleavage of Lignin Systems by Nitrogen Monoxide and Hydrazine

The cleavage of representative lignin systems has been achieved in a metal-free two-step sequence first employing nitrogen monoxide for oxidation followed by hydrazine for reductive C?O bond scission. In combining nitrogen monoxide and lignin, the newly developed valorization strategy shows the particular feature of starting from two waste materials, and it further exploits the attractive conditions of a Wolff-Kishner reduction for C?O bond cleavage for the first time. (Figure presented.).

Cross-coupling of hydroxycinnamyl aldehydes into lignins

(equation presented) Pathways for hydroxycinnamyl aldehyde incorporation into lignins are revealed by examining transgenic plants deficient in cinnamyl alcohol dehydrogenase, the enzyme that converts hydroxycinnamyl aldehydes to the hydroxycinnamyl alcoho