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Magnoshinin is a neolignan compound characterized by a 1,2-dihydronaphthalene structure substituted with a 2,4,5-trimethoxyphenyl group at position 1 (the 1S,2R stereoisomer), methyl groups at positions 2 and 3, and methoxy groups at positions 5, 7, and 8 respectively.

86702-02-5

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86702-02-5 Usage

Uses

Used in Pharmaceutical Industry:
Magnoshinin is used as a pharmaceutical agent for its potential therapeutic properties. It has been studied for its bioactive compounds, which may contribute to the development of new drugs and treatments.
Used in Natural Product Research:
Magnoshinin is utilized in the field of natural product research as a compound derived from plants. Its unique structure and potential biological activities make it a valuable subject for further investigation and potential applications in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 86702-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86702-02:
(7*8)+(6*6)+(5*7)+(4*0)+(3*2)+(2*0)+(1*2)=135
135 % 10 = 5
So 86702-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H30O6/c1-13-9-15-18(26-4)12-21(29-7)24(30-8)23(15)22(14(13)2)16-10-19(27-5)20(28-6)11-17(16)25-3/h9-12,14,22H,1-8H3/t14-,22-/m1/s1

86702-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name magnoshinin

1.2 Other means of identification

Product number -
Other names Magnoshinin

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:86702-02-5 SDS

86702-02-5Relevant articles and documents

Synthesis of magnoshinin and cyclogalgravin: Modified stobbe condensation reaction

Yvon,Datta,Le,Charlton

, p. 1556 - 1560 (2007/10/03)

The development of new methods for lignan synthesis is reported. A recently reported method for the preparation of 1-aryl-1,2-dihydronaphthalenes is exploited to prepare magnoshinin, a naturally occurring lignan, and cyclogalgravin (3,4-dehydrogalbulin), a derivative of a natural lignan.

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