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207446-83-1

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207446-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207446-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,4,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 207446-83:
(8*2)+(7*0)+(6*7)+(5*4)+(4*4)+(3*6)+(2*8)+(1*3)=131
131 % 10 = 1
So 207446-83-1 is a valid CAS Registry Number.

207446-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name arteanniun H

1.2 Other means of identification

Product number -
Other names arteannuin H

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:207446-83-1 SDS

207446-83-1Downstream Products

207446-83-1Relevant articles and documents

METHOD AND DEVICE FOR THE SYNTHESIS OF ARTEMISININ

-

Page/Page column 79; 80, (2013/03/28)

The present invention is directed to a method for producing artemisinin having the formula (6) from dihydroartennisinic acid in a continuous flow reactor using singlet oxygen as well as to the continuous flow reactor for producing artemisinin.

The mechanism of the spontaneous autoxidation of dihydroartemisinic acid

Sy, Lai-King,Brown, Geoffrey D

, p. 897 - 908 (2007/10/03)

Dihydroartemisinic acid undergoes slow spontaneous autoxidation to artemisinin and other natural products, which have been reported from the medicinal plant Artemisia annua. The mechanism of this complex transformation is shown to involve four steps: (i) initial reaction of the Δ4.5-double bond of dihydroartemisinic acid with molecular oxygen, (ii) Hock cleavage of the resulting tertiary allylic hydroperoxide; (iii) oxygenation of the enol product from Hock cleavage; and (iv) cyclization of the resulting vicinal hydroperoxyl-aldehyde to the 1,2,4-trioxane system of artemisinin.

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