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14882-64-5

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14882-64-5 Usage

General Description

1,3,3a,4,7,7-Alpha-Hexahydro-1,3-dimethoxy-4,7-methanoisobenzofuran is a chemical compound with a complex molecular structure. It belongs to the class of organic compounds known as lignans, which are natural substances found in plants. This particular compound is derived from the roots of the Japanese herb Schisandra chinensis and is known for its potential medicinal properties. It has been investigated for its possible anti-inflammatory, anticancer, and neuroprotective effects, although further research is needed to fully understand its pharmacological properties. The compound’s chemical structure and potential biological activities make it a subject of interest in the field of natural product chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 14882-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,8 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14882-64:
(7*1)+(6*4)+(5*8)+(4*8)+(3*2)+(2*6)+(1*4)=125
125 % 10 = 5
So 14882-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c1-12-10-8-6-3-4-7(5-6)9(8)11(13-2)14-10/h3-4,6-11H,5H2,1-2H3

14882-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,3a,4,7,7-α-Hexahydro-1,3-dimethoxy-4,7-methanoisobenzofuran

1.2 Other means of identification

Product number -
Other names 4,7-Methanoisobenzofuran,1,3,3a,4,7,7a-hexahydro-1,3-dimethoxy

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:14882-64-5 SDS

14882-64-5Relevant articles and documents

Formal synthesis of (±)-udoteatrial hydrate

Chang, Meng-Yang,Lin, Ching-Han,Chang, Nein-Chen

, p. 1581 - 1585 (2004)

The formal synthesis of antimicrobial diterpene udoteatrial hydrate (1) is described in nine steps. Diol 6 used as starting material. The key intermediate 4 was obtained from bicyclic ketone 5 via the key Norrish type I reaction.

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