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90822-23-4

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90822-23-4 Usage

Description

(3S,4R)-3-<(1R)-1-hydroxyethyl>-4-<(1R)-1-methyl-3-p-nitrobenzyloxycarbonyl-2-oxopropyl>-2-azetidin-2-one is a complex organic molecule characterized by a 2-azetidin-2-one ring with a hydroxyethyl group at the third carbon and a p-nitrobenzyloxycarbonyl-2-oxopropyl group at the fourth carbon. The molecule also features a methyl group at the first carbon, which, along with the other functional groups, endows the compound with diverse chemical properties. These properties make it a candidate for various applications, particularly in the fields of pharmaceuticals and organic synthesis.

Uses

Used in Pharmaceutical Industry:
(3S,4R)-3-<(1R)-1-hydroxyethyl>-4-<(1R)-1-methyl-3-p-nitrobenzyloxycarbonyl-2-oxopropyl>-2-azetidin-2-one is used as a pharmaceutical intermediate for the synthesis of complex drug molecules. Its unique structure and functional groups allow for the development of new therapeutic agents with potential applications in treating various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (3S,4R)-3-<(1R)-1-hydroxyethyl>-4-<(1R)-1-methyl-3-p-nitrobenzyloxycarbonyl-2-oxopropyl>-2-azetidin-2-one serves as a key building block for the creation of more complex organic compounds. Its versatile functional groups enable chemists to perform a range of reactions, leading to the formation of novel molecules with potential applications in various industries, such as materials science, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 90822-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,2 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90822-23:
(7*9)+(6*0)+(5*8)+(4*2)+(3*2)+(2*2)+(1*3)=124
124 % 10 = 4
So 90822-23-4 is a valid CAS Registry Number.

90822-23-4Upstream product

90822-23-4Relevant articles and documents

AN IMPROVED PROCESS FOR THE PREPARATION OF MEROPENEM

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, (2011/12/02)

The present invention provides an improved process for the preparation of methyl carbapenem derivative of formula (I) or its pharmaceutically acceptable salts or hydrates thereof in a pure form.

A PROCESS FOR THE PREPARATION OF MEROPENEM

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Page/Page column 15-16, (2010/11/28)

The invention relates to a process for the preparation of meropenem, a β-methylcarbopenem. The said process comprises the following steps: preparing the compound of Formula (XI) from the compound of Formula (IV) through three steps "one-pot process"; then condensing the compound of Formula (XI) with the compound of Formula (XX) to form the compound of Formula (XXIV); finally preparing meropenam of Formula (I) from the compound of Formula (XXIV) by deprotection reaction by means of catalyst. The process of the invention is easily to carry out, the product is isolated in high content and yield, and the cost is reduced, thereby overcoming the shortage of the prior art.

β-lactams. 1. Highly diastereoselective alkylation of 4-acetoxyazetidin-2-one useful for 1β-methylcarbapenem synthesis

Nagao,Kumagai,Nagase,Tamai,Inoue,Shiro

, p. 4232 - 4237 (2007/10/02)

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