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5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-8-oxo-, (6R)- is a complex organic compound with the chemical formula C10H11NO5S. It is a chiral molecule, with the (6R)- configuration indicating the specific arrangement of atoms in the molecule. 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid, 3-[(acetyloxy)methyl]-8-oxo-, (6R)- is characterized by a bicyclic ring structure, with a sulfur atom in the 5-position and a nitrogen atom in the 1-position. The molecule features a carboxylic acid group at the 2-position, an acetyloxymethyl group at the 3-position, and an oxo group at the 8-position. Due to its unique structure and properties, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid, 3-[(acetyloxy)methyl]-8-oxo-, (6R)- has potential applications in various fields, such as pharmaceuticals and chemical research.

4704-60-3

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4704-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4704-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4704-60:
(6*4)+(5*7)+(4*0)+(3*4)+(2*6)+(1*0)=83
83 % 10 = 3
So 4704-60-3 is a valid CAS Registry Number.

4704-60-3Upstream product

4704-60-3Downstream Products

4704-60-3Relevant academic research and scientific papers

Process for P-nitrobenzyl ester cleavage in cephalosporin

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, (2008/06/13)

A process for converting cephalosporin p-nitrobenzyl ester (Formula I) to the corresponding cephalosporin free acid (Formula II) comprising treating the cephalosporin p-nitrobenzyl ester with a metal selected from the group consisting of iron, magnesium, aluminum, and tin, and with hydrochloric acid in a mixture of water and a water-miscible organic solvent. Preferably, the metal is iron in the form of a fine powder, and the reaction is carried out at a temperature in the range of 30°-50° C.

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