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807363-10-6

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807363-10-6 Usage

Uses

The S-enantiomer of Arundic Acid. An astrocyte modulating agent, in acute ischemic stroke.

Check Digit Verification of cas no

The CAS Registry Mumber 807363-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,6 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 807363-10:
(8*8)+(7*0)+(6*7)+(5*3)+(4*6)+(3*3)+(2*1)+(1*0)=156
156 % 10 = 6
So 807363-10-6 is a valid CAS Registry Number.

807363-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(+)-arundic acid

1.2 Other means of identification

Product number -
Other names S-(+)-Arundic Acid

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:807363-10-6 SDS

807363-10-6Downstream Products

807363-10-6Relevant articles and documents

A concise and efficient route to the Alzheimer's therapeutic agent (R)-arundic acid

García, Jesús M.,Odriozola, José M.,Lecumberri, Ainara,Razkin, Jesús,González, Alberto

, p. 10664 - 10669 (2008/12/23)

A short and efficient procedure for the preparation of (R)-arundic acid, a therapeutic agent for the treatment of Alzheimer's disease, has been developed. Based on cheap and commercially available (1R)-(+)-camphor as the source of chiral information, (R)-arundic acid is synthesized in a four-step cyclic sequence with 55% overall yield and high optical purity, ≥98% ee. Alkyl halide and acetylene constitute the only consumable carbon sources of this method, which allows obtaining of both enantiomers and recycling of chiral auxiliary.

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