7460-41-5

Basic information

• Product Name: (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate
• CAS NO: 7460-41-5
• Molecular Formula: C₂₂H₂₂O₇
• Molecular Weight: 398.4059
• Mol File: 7460-41-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 580.6°C at 760 mmHg
• Flash Point: 253°C
• Density: 1.249g/cm³
• Vapor Pressure: 1.79E-13mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate(7460-41-5)
• EPA Substance Registry System: (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate(7460-41-5)

Safety Data

• Hazardous Substances Data: 7460-41-5(Hazardous Substances Data)

Usage

Description

(2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate is an ester compound that features two aromatic rings. It consists of a (1,3-benzodioxol-5-yl)prop-2-en-1-yl group, which is derived from 1,3-benzodioxole, and a 3-(3,4,5-trimethoxyphenyl)prop-2-enoate group that includes three methoxy (CH3O-) groups attached to a phenyl ring. This chemical structure may endow it with unique biological and chemical properties, making it a candidate for applications in fields such as pharmaceuticals, cosmetics, or agrochemicals.

Uses

Used in Pharmaceutical Industry:
(2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate is used as a pharmaceutical compound for its potential biological activity. The presence of aromatic rings and methoxy groups may contribute to its interaction with biological targets, offering possible applications in the development of new drugs.
Used in Cosmetics Industry:
In the cosmetics industry, (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate is used as an ingredient for its potential benefits to skin health. (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate's structure may provide antioxidant properties or contribute to the formulation of cosmetic products with improved efficacy.
Used in Agrochemicals Industry:
(2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate is utilized as an agrochemical compound for its potential applications in pest control or plant protection. (2E)-3-(1,3-benzodioxol-5-yl)prop-2-en-1-yl 3-(3,4,5-trimethoxyphenyl)prop-2-enoate's chemical properties might enable it to be developed into new products that enhance crop yield or protect against various agricultural threats.

Upstream product

• 20329-98-0 (E)-3,4,5-trimethoxy-cinnamic acid 
• 58095-76-4 (E)-3-(benzo[d][1,3]dioxol-5-yl)prop-2-en-1-ol 

Downstream Products

• 103844-22-0 1,3,3aβ,4β,9β,9aα-hexahydro-4α-hydroxy-6,7,8-trimethoxy-9α-(3,4-methylenedioxyphenyl)naphtho<2,3-c>furan-3-one 
• 118826-03-2 1,3,9β,9aα-tetrahydro-6,7,8-trimethoxy-9α-(3,4-methylenedioxyphenyl)naphtho<2,3-c>furan-3-one 

Relevant articles and documents

A new synthesis of podophyllum lignans by Weitz' aminium salt-induced free radical cycloaddition reaction of a doubly unsaturated ester

(±)-Isopodophyllotoxin (1e) and related lactones 12, 13, 14 were synthesized by a biomimetic procedure from the doubly unsaturated esters 11a and 11b by means of an oxidative free radical cycloaddition reaction utilizing a stable cation radical salt, Weitz' aminium salt, in one step. (±)-Isopicropodophyllin (1g), the trans-fused lactones, 12, 13, and 16, and the cis-fused lactone 17 were also synthesized from the esters 11c and 11d by the reaction with the same reagent.