112601-22-6

Basic information

• Product Name: 7-(2-(2-aminothiazolyl)-2-methoxyiminoacetamido)-3-(imidazo(1,2-a)pyridinium-1-yl)methyl-3-cephem-4-carboxylate
• Synonyms: 7-(2-(2-aminothiazolyl)-2-methoxyiminoacetamido)-3-(imidazo(1,2-a)pyridinium-1-yl)methyl-3-cephem-4-carboxylate
• CAS NO: 112601-22-6
• Molecular Formula: C21H19 N7 O5 S2
• Molecular Weight: 0
• Mol File: 112601-22-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 7-(2-(2-aminothiazolyl)-2-methoxyiminoacetamido)-3-(imidazo(1,2-a)pyridinium-1-yl)methyl-3-cephem-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(2-(2-aminothiazolyl)-2-methoxyiminoacetamido)-3-(imidazo(1,2-a)pyridinium-1-yl)methyl-3-cephem-4-carboxylate(112601-22-6)
• EPA Substance Registry System: 7-(2-(2-aminothiazolyl)-2-methoxyiminoacetamido)-3-(imidazo(1,2-a)pyridinium-1-yl)methyl-3-cephem-4-carboxylate(112601-22-6)

Safety Data

• Hazardous Substances Data: 112601-22-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C21H19N7O5S2/c1-33-25-14(12-10-35-21(22)23-12)17(29)24-15-18(30)28-16(20(31)32)11(9-34-19(15)28)8-27-7-6-26-5-3-2-4-13(26)27/h2-7,10,15,19H,8-9H2,1H3,(H3-,22,23,24,29,31,32)/b25-14+/t15-,19-/m0/s1

Upstream product

• 274-76-0 imidazo[1,2-a]pyridine 
• 152186-44-2 7β-[2-(2-aminothiazol-4-yl)-2-(Z)-methoxyiminoacetamido]-3-hydroxymethyl-3-cephem-4-carboxylic acid 
• 121020-94-8 7β-((Z)-(2-amino-1,3-thiazol-4-yl)-2-methoximinoacetamido)-3-hydroxymethyl-3-cephem-4-carboxylic acid 
• 64-17-5 ethanol 
• 702-86-3 Methyl-o-phenylenphosphat 
• 152186-43-1 7β-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetoamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid 

Relevant articles and documents

Method for production of cephalosporin compounds

A method for producing a compound of the formula; STR1 wherein R stands for a hydrogen atom, an acyl group or a protective group other than acyl groups, Q stands for a hydrogen atom or an ester residue, Y stands for the residue of a nucleophilic compound and the dotted line shows the double bond at 2- or 3- position of the cephem ring or a salt thereof, characterized by allowing a compound of the formula; STR2 [R, Q and the dotted line are of the same meaning as above] or a salt thereof to react with a nucleophilic compound or a salt thereof and a compound of the formula; STR3 wherein R1, R2, R3 independently stand for a hydrocarbon group having not more than 8 carbon atoms, or R1 and R2, R1 and R3 or R2 and R3 may be combined to form polymethylene group, according to which the end product [I] of high quality can be provided in a high yield by one reaction step by using the compound [III] of relatively low cost, thus the method of this invention is advantageous for mass-producing the compound [I] on an industrial scale from the compound [II] and a nucleophilic compound.