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83708-70-7

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83708-70-7 Usage

General Description

Dihydrosesamin is a chemical compound derived from the natural product rosmarinic acid, a polyphenol found in various plants, including rosemary. It is known for its antioxidant and anti-inflammatory properties, and has been studied for its potential therapeutic applications in the treatment of neurological disorders, such as Alzheimer's disease and Parkinson's disease, as well as in the management of cardiovascular diseases and diabetes. Dihydrosesamin has also been reported to possess anti-cancer properties, with potential use in cancer therapy. Overall, dihydrosesamin shows promise as a versatile compound with various potential health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 83708-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,0 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83708-70:
(7*8)+(6*3)+(5*7)+(4*0)+(3*8)+(2*7)+(1*0)=147
147 % 10 = 7
So 83708-70-7 is a valid CAS Registry Number.

83708-70-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ((2R,3S,4S)-2-(benzo[d][1,3]dioxol-5-yl)-4-(benzo[d][1,3]dioxol-5-ylmethyl)tetrahydrofuran-3-yl)methanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83708-70-7 SDS

83708-70-7Downstream Products

83708-70-7Relevant articles and documents

A sterically encumbered photoredox catalyst enables the unified synthesis of the classical lignan family of natural products

Alfonzo, Edwin,Beeler, Aaron B.

, p. 7746 - 7754 (2019/08/30)

Herein, we detail a unified synthetic approach to the classical lignan family of natural products that hinges on divergence from a common intermediate that was strategically identified from nature's biosynthetic blueprints. Efforts toward accessing the common intermediate through a convergent and modular approach resulted in the discovery of a sterically encumbered photoredox catalyst that can selectively generate carbonyl ylides from electron-rich epoxides. These can undergo concerted [3 + 2] dipolar cycloadditions to afford tetrahydrofurans, which were advanced (2-4 steps) to at least one representative natural product or natural product scaffold within all six subtypes in classical lignans. The application of those synthetic blueprints to the synthesis of heterolignans bearing unnatural functionality was demonstrated, which establishes the potential of this strategy to accelerate structure-activity-relationship studies of these natural product frameworks and their rich biological activity.

Reagent-controlled stereoselective synthesis of lignan-related tetrahydrofurans

Miles, Steven M.,Marsden, Stephen P.,Leatherbarrow, Robin J.,Coates, William J.

, p. 6874 - 6882 (2007/10/03)

The reaction of ring-closing metathesis-derived cyclic allylsiloxanes 3 with aldehydes in the presence of a Lewis acid gives 2,3,4-trisubstituted tetrahydrofurans related to the furanolignan family of natural products. The reactions proceed with complete

Stereoselective synthesis of trisubstituted tetrahydrofurans by radical cyclisation reaction using a hypophosphite salt. Application to the total synthesis of (±)-dihydrosesamin

Chandra Roy, Subhas,Guin, Chandrani,Kumar Rana, Kalyan,Maiti, Gourhari

, p. 2435 - 2439 (2007/10/03)

The stereoselective synthesis of tetrahydrofurans has been achieved from bromoalkynes and bromoalkenes by intramolecular radical cyclisation using a hypophosphite salt. This radical cyclisation strategy has successfully been applied to the total synthesis

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