Your Location:Home >Products >API >122547-49-3

122547-49-3

  • Product NameFaropenem sodium
  • Molecular FormulaC12H14NNaO5S
  • Molecular Weight307.303
  • Purity99%
  • Appearancepale yellow crystals
Inquiry

Product Details

Quick Details

  • CasNo: 122547-49-3
  • Molecular Formula: C12H14NNaO5S
  • Appearance: pale yellow crystals
  • Purity: 99%

Chinese Factory Supply  Top Purity 99% Faropenem sodium 122547-49-3 with Safe Transportation

  • Molecular Formula:C12H14NNaO5S
  • Molecular Weight:307.303
  • Appearance/Colour:pale yellow crystals 
  • Vapor Pressure:2.23E-15mmHg at 25°C 
  • Boiling Point:570.2 °C at 760 mmHg 
  • Flash Point:298.7 °C 
  • PSA:115.20000 
  • LogP:-1.02310 

Faropenem sodium(Cas 122547-49-3) Usage

Chemical Properties

Pale Yellow Crystals

Uses

Faropenem is an orally active beta-lactam antibiotic belonging to the penem group.

General Description

Faropenem sodium hydrate belongs to the penem group of antibiotics prescribed for oral usage. Enterobacteriaceae bacterial infections with cephalosporin resistance are susceptible to faropenem. Faropenem could be an effective antibiotic to treat urinary tract infections caused by extended-spectrum beta-lactamases (ESBL) producing bacteria.

Biochem/physiol Actions

Faropenem sodium is an ultra-broad spectrum, β-lactamase resistant, β-lactam antibiotic active against both Gram-positive and Gram-negative bacteria.

InChI:InChI=1/C12H15NO5S.Na/c1-5(14)7-10(15)13-8(12(16)17)9(19-11(7)13)6-3-2-4-18-6;/h5-7,11,14H,2-4H2,1H3,(H,16,17);/q;+1/p-1/t5-,6-,7+,11-;/m1./s1

122547-49-3 Relevant articles

An efficient method for removal of residual palladium from organic solution of faropenem sodium in the Pd(II)-catalyzed cleavage of allyl faropenem

Huang, Jian-Ping,Chen, Xu-Xiang,Gu, Shuang-Xi,Zhao, Lei,Chen, Wen-Xue,Chen, Fen-Er

, p. 939 - 941 (2010)

An improved palladium(II)-catalyzed clea...

New intermediate of faropenem sodium as well as preparation method and application thereof (by machine translation)

-

, (2019/09/17)

The intermediate is easy to prepare, low...

Preparation method of faropenem sodium

-

Paragraph 0052; 0086-0094; 0110-0112, (2017/12/06)

The invention discloses a preparation me...

A synthesis method of faropenem sodium

-

, (2017/07/14)

The invention provides a method for synt...

122547-49-3 Process route

(5R,6S)-6-((R)-1-hydroxyethyl)-2-((R)-tetrahydro-2-furyl)penem-3-carboxylic acid allyl ester
106559-80-2

(5R,6S)-6-((R)-1-hydroxyethyl)-2-((R)-tetrahydro-2-furyl)penem-3-carboxylic acid allyl ester

Furopenem
122547-49-3

Furopenem

Conditions
Conditions Yield
With bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine; sodium 2-ethylhexanoic acid; In water; ethyl acetate; at 20 ℃; for 5h; Inert atmosphere; Large scale reaction;
86.5%
(5R,6S)-6-((R)-1-hydroxyethyl)-2-((R)-tetrahydro-2-furyl)penem-3-carboxylic acid allyl ester; With sodium isooctanoate; sodium caprylate; triphenylphosphine; In dichloromethane; ethyl acetate; at 20 ℃;
With tetrakis(triphenylphosphine) palladium(0); In dichloromethane; ethyl acetate; at 25 - 30 ℃; for 0.666667h; Inert atmosphere;
73.3%
With tetrakis(triphenylphosphine) palladium(0); triphenylphosphine; sodium 2-ethylhexanoic acid; In ethyl acetate; for 1h; Ambient temperature;
 
faropenem
106560-14-9,106560-15-0

faropenem

Furopenem
122547-49-3

Furopenem

Conditions
Conditions Yield
With sodium 2-ethylhexanoic acid; In tetrahydrofuran; water; at 20 ℃; for 2h;
125 g

122547-49-3 Upstream products

  • 106559-80-2
    106559-80-2

    (5R,6S)-6-((R)-1-hydroxyethyl)-2-((R)-tetrahydro-2-furyl)penem-3-carboxylic acid allyl ester

  • 76899-07-5
    76899-07-5

    (3R,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-acetoxyazetidin-2-one

  • 153165-72-1
    153165-72-1

    R-(+)-thio tetrahydrofuran-2-carboxylic acid

  • 106560-32-1
    106560-32-1

    (R)-Tetrahydro-furan-2-carbothioic acid S-{(2R,3S)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl} ester

122547-49-3 Downstream products

  • 133885-56-0
    133885-56-0

    Sodium; (5S,6S)-6-((R)-1-hydroxy-ethyl)-7-oxo-3-(R)-tetrahydro-furan-2-yl-4-thia-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylate

;