102772-66-7 Usage
Description
1-[[(6R,7R)-7-[[(2Z)-2-(2-AMino-4-thiazolyl)-2-[[2-(1,1-diMethylethoxy)-1,1-diMethyl-2-oxoethoxy]iMino]acetyl]aMino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]Methyl]pyridiniuM Inner Salt is a complex organic compound with a unique molecular structure. It is characterized by its heterocyclic ring systems and various functional groups, which may contribute to its potential applications in different fields.
Uses
1. Used in Pharmaceutical Applications:
1-[[(6R,7R)-7-[[(2Z)-2-(2-AMino-4-thiazolyl)-2-[[2-(1,1-diMethylethoxy)-1,1-diMethyl-2-oxoethoxy]iMino]acetyl]aMino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]Methyl]pyridiniuM Inner Salt is used as an active pharmaceutical ingredient (API) for the development of new drugs targeting various diseases and conditions. Its unique molecular structure and functional groups may provide novel mechanisms of action and therapeutic benefits.
2. Used in Chemical Research:
1-[[(6R,7R)-7-[[(2Z)-2-(2-AMino-4-thiazolyl)-2-[[2-(1,1-diMethylethoxy)-1,1-diMethyl-2-oxoethoxy]iMino]acetyl]aMino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]Methyl]pyridiniuM Inner Salt can be utilized in chemical research as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups may offer new insights into chemical reactions and mechanisms, potentially leading to the discovery of new compounds with specific applications.
3. Used in Material Science:
The compound's structural features and properties may make it suitable for use in the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity. It could be employed in the design of catalysts, sensors, or other advanced materials.
Please note that the provided materials do not mention any specific uses for Glycerol. The uses listed above are based on the general properties and potential applications of the described compound.
Check Digit Verification of cas no
The CAS Registry Mumber 102772-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,7 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102772-66:
(8*1)+(7*0)+(6*2)+(5*7)+(4*7)+(3*2)+(2*6)+(1*6)=107
107 % 10 = 7
So 102772-66-7 is a valid CAS Registry Number.
102772-66-7Relevant articles and documents
General Synthesis of Industrial Cephalosporin-Based Antibiotics Through Amidation with Tosyl Chloride as a Coupling Reagent
Pieper, Matthias,Schleich, Herbert,Gr?ger, Harald
, p. 3259 - 3263 (2019)
In this contribution we demonstrate the feasibility of a recently developed amidation method for a general synthesis of industrially important semi-synthetic cephalosporin antibiotics starting from readily available 7-aminocephalosporanic acid and derivatives thereof. The amidation process is based on the use of 4-toluene-sulfonyl chloride as an economically attractive coupling reagent in combination with methanol or ethyl acetate as one of the solvent components. A broad reaction scope was shown by the successful synthesis of three further cephalosporin antibiotics with different functionalities, which were obtained in high yields of 82–95 % in the reactions even under non-optimized conditions. It is noteworthy that also different oxime functionalities in the side chain of the 7′-position are tolerated as well as an ester moiety in 4′-position and a cationic functionality in 3′-position. Thus, this amidation process through an activated anhydride formed by means of 4-toluenesulfonyl chloride is a broadly applicable methodology for the synthesis of industrial semi-synthetic cephalosporin antibiotics.
IMPROVED PROCESS FOR THE PREPARATION OF CEPHALOSPORIN ANTIBIOTICS
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Page/Page column 12-13, (2008/06/13)
Abstract The present invention more particularly relates to a process for the preparation of cephalosporin antibiotics of the Formula (I) wherein R1 represents hydrogen, trityl, alkyl like CH3, CRaRbCOORc where Ra and Rb independently represent hydrogen or methyl and Rc represents hydrogen or (C1-C6) alkyl; R2 is carboxylate ion or COORd, where Rd represents hydrogen, ester or a counter ion which forms a salt; R3 represents hydrogen, CH3, CH2OCH3, CH2OCOCH3, CH=CH2, Formula (II).
