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The chemical compound "5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)-(methoxyimino)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, [6R-[6R,7α(E)]]-" is a complex, cyclic molecule with a unique structure. It features a 5-thia-1-azabicyclo[4.2.0]octane core, which is a type of bicyclic ring system containing sulfur. The molecule is further characterized by a carboxylic acid group at the 2-position, a 7-position substituted with a complex amino-acetyl group, and a 3-position with a methyl-tetrazol-5-yl-thiomethyl group. The 8-oxo group indicates the presence of a carbonyl group at the 8-position, and the [6R-[6R,7α(E)]]- notation specifies the stereochemistry of the molecule, indicating that the 6-position has the R configuration, and the double bond at the 7α position is in the E configuration. 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2- carboxylic acid,7-[[(2-amino-4-thiazolyl)- (methoxyimino)acetyl]amino]-3-[[(1-methyl- 1H-tetrazol-5-yl)thio]methyl]-8-oxo-,[6R- [6R,7â(E)]]- is likely to have specific biological activity or be used in pharmaceutical applications due to its intricate structure and functional groups.

66340-45-2

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66340-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66340-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,4 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66340-45:
(7*6)+(6*6)+(5*3)+(4*4)+(3*0)+(2*4)+(1*5)=122
122 % 10 = 2
So 66340-45-2 is a valid CAS Registry Number.

66340-45-2Downstream Products

66340-45-2Relevant academic research and scientific papers

Diethyl chlorophosphate: An effective and convenient coupling reagent of cephalosporin derivatives

Lee, Hong-Woo,Kang, Tae Won,Cha, Kyung Hoi,Kim, Eung-Nam,Choi, Nam-Hee,Kim, Jung-Woo,Hong, Chung Il

, p. 35 - 44 (1998)

A coupling reagent, diethyl chlorophosphate (DECP) 2, was reacted with 2-(2-amino-4-thiazolyl)-2-syn-alkoxyiminoacetic acid 1 to give an active ester intermediate 3.

Alkyloximes of 7-amino-thiazolyl-acetamido-cephalosporanic acids

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, (2008/06/13)

Novel alkyloximes of 7-amino-thiazolyl-acetamidocephalosporanic acids of the formula STR1 wherein R is selected from the group consisting of alkyl of 1 to 5 carbon atoms, cycloalkyl of 3 to 5 carbon atoms and --CH2 --SR', R' is selected from the group consisting of acyl of an alkanoic acid of 2 to 4 carbon atoms, 1-methyl-tetrazolyl and 2-methyl-1,3,4-thiadiazolyl, R1 is selected from the group consisting of hydrogen and a group easily removeable by acid hydrolysis or hydrogenolysis, R2 is selected from the group consisting of alkyl of 1 to 4 carbon atoms and alkenyl and alkynyl of 2 to 4 carbon atoms, A is selected from the group consisting of hydrogen, an alkali metal cation, an equivalent of an alkaline earth metal or magnesium, an organic amine base cation and an ester group easily removeable by acid hydrolysis or hydrogenolysis with the proviso that when R1 is hydrogen, A is not an ester group easily removeable by hydrogenolysis or acid hydrolysis and the wavy line means that OR2 is in one or the other of the two possible syn or anti isomeric positions having a very good antibiotic activity and novel processes and intermediates for their preparation.

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