1192650-82-0 Usage
Description
(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octan-2-carboxylic acid benzyl ester is a chiral benzyl ester derivative of a bicyclic compound that features a diazabicyclo[3.2.1]octane ring system. It is characterized by a carboxylic acid group, a benzyl ester group, and a cyclic structure with a ketone and benzyloxy substituents. The S and R designations denote the stereochemistry at the 2nd and 5th positions within the diazabicyclo[3.2.1]octane ring, which is crucial for its potential applications in organic chemistry and pharmaceutical research.
Uses
Used in Organic Synthesis:
(2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octan-2-carboxylic acid benzyl ester is used as a protecting group for carboxylic acids in organic synthesis. The benzyl ester moiety allows for selective modification of other functional groups within a molecule, facilitating complex organic reactions and the synthesis of pharmaceutical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octan-2-carboxylic acid benzyl ester is utilized as a key intermediate in the development of new drugs. Its unique structure and chirality make it a promising candidate for the synthesis of biologically active molecules, potentially leading to the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1192650-82-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,6,5 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1192650-82:
(9*1)+(8*1)+(7*9)+(6*2)+(5*6)+(4*5)+(3*0)+(2*8)+(1*2)=160
160 % 10 = 0
So 1192650-82-0 is a valid CAS Registry Number.
1192650-82-0Relevant articles and documents
B-LACTAMASE INHIBITOR AND APPLICATION THEREOF
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, (2018/03/07)
The present invention relates to a compound of Formula (I)-(IV) useful as β-lactamase inhibitor, a pharmaceutically acceptable salt, ester, solvate or stereoisomer thereof, wherein R1, R2, M and ring A have definitions as those in the specification. The present invention further relates to methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and uses of these compounds. For example, the compounds of the present invention can be used as β-lactamase inhibitors, for treatment and/or prophylaxis of diseases caused by bacterial infections, solving drug-resistance problems caused by β-lactamases, especially bacterial drug-resistant diseases caused by type B metallo-β-lactamases.
SODIUM SALT OF (2S, 5R)-6-BENZYLOXY-7-OXO-1,6-DIAZA-BICYCLO [3.2.1 ] OCTANE-2-CARBOXYLIC ACID AND ITS PREPARATION
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Page/Page column 6; 10, (2014/09/29)
Sodium salt of (2S, 5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2- carboxylic acid and a process for its preparation is disclosed.
PROCESSES FOR PREPARING HETEROCYCLIC COMPOUNDS INCLUDING TRANS-7-OXO-6-(SULPHOOXY)-1,6-DIAZABICYCLO[3,2,1]OCTANE-2-CARBOXAMIDE AND SALTS THEREOF
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, (2013/02/27)
The present invention relates to compounds and processes for preparing compounds of Formula (I), including compounds such as trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and salts thereof (e.g., NXL-104).
