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1206102-07-9

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1206102-07-9 Usage

Description

Methyl 3-(benzyloxy)-1-(2,3-dihydroxypropyl)-4-oxo-1,4-dihydropyridine-2-carboxylate is a complex organic compound with a unique chemical structure. It is characterized by its dihydropyridine core, which is a type of chemical structure commonly found in various biologically active compounds. The molecule features a benzyloxy group, two hydroxypropyl groups, and a carboxylate group, which contribute to its specific properties and potential applications.

Uses

1. Pharmaceutical Industry:
Methyl 3-(benzyloxy)-1-(2,3-dihydroxypropyl)-4-oxo-1,4-dihydropyridine-2-carboxylate is used as an intermediate in the synthesis of Dolutegravir (D528800), a second-generation HIV-1 integrase strand transfer inhibitor. This application is due to its role in the development of a potent and effective antiretroviral drug, which is crucial in the fight against HIV/AIDS.
2. Drug Synthesis:
In the field of drug synthesis, Methyl 3-(benzyloxy)-1-(2,3-dihydroxypropyl)-4-oxo-1,4-dihydropyridine-2-carboxylate serves as a key building block for the creation of various pharmaceutical compounds. Its unique structure allows for further chemical modifications and functionalization, making it a valuable asset in the development of new drugs with potential therapeutic applications.
While the provided materials do not explicitly mention other industries or applications for Methyl 3-(benzyloxy)-1-(2,3-dihydroxypropyl)-4-oxo-1,4-dihydropyridine-2-carboxylate, its chemical structure and properties suggest that it may have potential uses in other areas, such as materials science or chemical research. Further investigation and experimentation would be necessary to explore these possibilities.

Check Digit Verification of cas no

The CAS Registry Mumber 1206102-07-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,1,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1206102-07:
(9*1)+(8*2)+(7*0)+(6*6)+(5*1)+(4*0)+(3*2)+(2*0)+(1*7)=79
79 % 10 = 9
So 1206102-07-9 is a valid CAS Registry Number.

1206102-07-9SDS

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 2-?Pyridinecarboxylic acid, 1-?(2,?3-?dihydroxypropyl)?-?1,?4-?dihydro-?4-?oxo-?3-?(phenylmethoxy)?-?, methyl ester

1.2 Other means of identification

Product number -
Other names -

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:1206102-07-9 SDS

1206102-07-9Relevant articles and documents

Practical Synthetic Method for the Preparation of Pyrone Diesters: An Efficient Synthetic Route for the Synthesis of Dolutegravir Sodium

Yasukata, Tatsuro,Masui, Moriyasu,Ikarashi, Fumiya,Okamoto, Kazuya,Kurita, Takanori,Nagai, Masahiko,Sugata, Yoshihide,Miyake, Naoki,Hara, Shinichiro,Adachi, You,Sumino, Yukihito

, p. 565 - 570 (2019/03/26)

A highly efficient and practical synthetic method for the preparation of pyrone diesters was established. The pyrone diester 3c can be prepared from readily available starting materials on a multihundred gram scale. The pyrone diester 3c can easily be converted to dolutegravir sodium (1). The synthetic route demonstrated herein provides an efficient and atom-economical synthetic method for preparing this potent anti-HIV agent.

Improved method for synthesizing dolutegravir

-

, (2019/03/30)

The invention relates to an improved method for synthesizing dolutegravir and belongs to the field of medicinal chemistry. The method takes maltol (compound 1) as a raw material, and a target is synthesized by the following route. The process raw material is cheap and easy to obtain, a reaction solvent can be recycled, the post-treatment operation is simple, the yield and the purity are high, especially the carbamoylation and debenzylation reaction are carried out in one step, the synthesis route is simplified, the cost is reduced, and the large-scale industrial production is facilitated.

Synthesis of carbamoylpyridone HIV integrase inhibitors and intermediates

-

, (2016/02/12)

A synthesis approach providing an early ring attachment via a bromination to compound 1-1 yielding compound II-II, whereby a final product such as AA can be synthesized. In particular, the 2,4-difluorophenyl-containing sidechain is attached before creation of the additional ring Q.

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