29126-11-2 Usage
Description
(6R,7R)-3-Methyl-8-oxo-7-phenylacetylamino-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 4-methoxy-benzyl ester is a complex organic compound characterized by its bicyclic ring system, derived from a carboxylic acid and a 4-methoxy-benzyl ester. It also features a phenylacetylamino group and a thia-aza group, which contribute to its potential as a versatile building block for the synthesis of other compounds. This chemical's specific properties and activities are yet to be fully explored, but it holds promise for applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
(6R,7R)-3-Methyl-8-oxo-7-phenylacetylamino-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 4-methoxy-benzyl ester is used as a building block for the synthesis of various pharmaceutical compounds due to its complex molecular structure and the presence of multiple functional groups.
Used in Chemical Industry:
In the chemical industry, (6R,7R)-3-Methyl-8-oxo-7-phenylacetylamino-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 4-methoxy-benzyl ester is used as an intermediate in the production of other complex organic molecules, taking advantage of its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 29126-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,2 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29126-11:
(7*2)+(6*9)+(5*1)+(4*2)+(3*6)+(2*1)+(1*1)=102
102 % 10 = 2
So 29126-11-2 is a valid CAS Registry Number.
29126-11-2Relevant articles and documents
A facile synthesis of 7-amino-3-desacetoxycephalosporanic acid derivatives by indium-mediated reduction of 3-iodomethylcephems in aqueous media
Chae, Hyungsun,Cho, Sangwon,Keum, Gyochang,Kang, Soon Bang,Pae, Ae Nim,Kim, Youseung
, p. 3899 - 3901 (2007/10/03)
An efficient reductive conversion of 3-iodomethylcephalosporin and 3- acetoxymethylcephalosporin derivatives mediated by indium into the corresponding 3-methylcephems and 3-methylenecephams in moderate to good yields has been developed in an aqueous system. 3-Methylenecephams are converted into the corresponding 3-methylcephems under previously reported basic conditions quantitatively. (C) 2000 Elsevier Science Ltd.
Palladium Catalysis in Cephalosporin Chemistry: General Methodology for the Synthesis of Cephem Side Chains
Farina, Vittorio,Baker, Stephen R.,Benigni, Daniel A.,Hauck, Sheila I.,Sapino, Chester
, p. 5833 - 5847 (2007/10/02)
We describe in full the palladium-catalyzed coupling of 3-(triflyloxy)cephems with organotin compounds, leading to the synthesis of 3-alkenyl-, 3-alkynyl-, and 3-arylcephems under exceptionally mild conditions.While this approach was not satisfactory for
Penicillin-cephalosporin conversion. XII. Electroreductive dechlorination of 3'-chlorocephalosporins into 3-methylenecephams
Torii,Tanaka,Ohshima,Sasaoka
, p. 3975 - 3976 (2007/10/02)
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