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471295-98-4

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471295-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 471295-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,1,2,9 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 471295-98:
(8*4)+(7*7)+(6*1)+(5*2)+(4*9)+(3*5)+(2*9)+(1*8)=174
174 % 10 = 4
So 471295-98-4 is a valid CAS Registry Number.

471295-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(5-ethylpyridin-2-yl)-2-hydroxyethoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-[2-(5-ethyl-pyridin-2-yl)-2-hydroxy-ethoxy]-benzaldehyde

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:471295-98-4 SDS

471295-98-4Relevant articles and documents

NOVEL PROCESS TO PREPARE PIOGLITAZONE VIA SEVERAL NOVEL INTERMEDIATES

-

Page/Page column 0079, (2014/04/03)

A novel process for preparing thiazolidinediones, preferably Pioglitazone, as described. Also described are novel intermediates involved in its synthesis and process for their preparation and use in medicine.

Process development and scale-up of the potential thiazolidinedione antidiabetic candidate PNU-91325

Carpenter, Donald E.,Imbordino, Rick J.,Maloney, Mark T.,Moeslein, Jeffery A.,Reeder, Michael R.,Scott, Allen

, p. 721 - 728 (2013/09/06)

An efficient six-step synthesis has been developed for the preparation of the thiazolidinedione analogue PNU-91325 (3) from the commercially available olefin 12. This process involves a novel epoxide ring opening with a deactivated phenol under phase-transfer conditions. Significant improvements were made in the oxidation of a secondary alcohol to the ketone and the 1,4-reduction of an enone from a previous process. Overall, this route allows for the preparation of PNU-91325 in 25% yield.

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