96087-10-4

Basic information

• Product Name: Massoniresil
• Synonyms: Massoniresil;Massoniresinol
• CAS NO: 96087-10-4
• Molecular Formula: C₂₀H₂₄O₈
• Molecular Weight: 392.39976
• Product Categories: Lignans
• Mol File: 96087-10-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 647.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.419±0.06 g/cm3(Predicted)
• PKA: 9.91±0.35(Predicted)
• CAS DataBase Reference: Massoniresil(CAS DataBase Reference)
• NIST Chemistry Reference: Massoniresil(96087-10-4)
• EPA Substance Registry System: Massoniresil(96087-10-4)

Safety Data

• Hazardous Substances Data: 96087-10-4(Hazardous Substances Data)

Usage

General Description

Massoniresil is a class of chemicals known as acrylates, widely used in various industrial and commercial applications. These chemicals have excellent adhesion and durability properties, making them ideal for use in the production of various coatings, adhesives, and sealants. They are also known for their strong resistance to environmental factors, such as UV radiation, moisture, and temperature changes. Massoniresil chemicals are also used in the production of rubber and plastics, where their flexibility and strength are highly valued. Due to their versatile nature and diverse applications, Massoniresil chemicals are an important component in many different industries, including construction, automotive, and electronics.

Relevant articles and documents

Absolute stereostructures and syntheses of saussureamines A, B, C, D and E, amino acid-sesquiterpene conjugates with gastroprotective effect, from the roots of Saussurea lappa

From the methanolic extract of the dried roots of Saussurea lappa Clarke, Saussureae Radix, five amino acid-sesquiterpene conjugates, saussureamines A, B, C, D and E, were isolated together with a lignan glycoside, (-)-massoniresinol 4-O-β-D-glucopyranoside. Their stereostructures were determined on the basis of chemical and physicochemical evidence. In addition, saussureamines and the related amino acid-sesquiterpene conjugates were synthesized using a Michael type addition reaction of amino acid to the α-methylene-γ-lactone moiety of sesquiterpenes. Saussureamines A, B and C, costunolide and dehydrocostus lactone showed a gastroprotective effect on acidified ethanol-induced gastric mucosal lesions in rats. Saussureamines A also exhibited an inhibitory effect on gastric mucosal lesions induced by water-immersion stress in mice. (C) 2000 Elsevier Science Ltd.