28180-92-9

Basic information

• Product Name: N-Boc-Cephalexin
• Synonyms: N-Boc-Cephalexin;N-tert-Butoxycarbonylcephalexin
• CAS NO: 28180-92-9
• Molecular Formula: C₂₁H₂₅N₃O₆S
• Molecular Weight: 447.5047
• Product Categories: Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 28180-92-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Solubility: Dimethyl Sulfoxide
• CAS DataBase Reference: N-Boc-Cephalexin(CAS DataBase Reference)
• NIST Chemistry Reference: N-Boc-Cephalexin(28180-92-9)
• EPA Substance Registry System: N-Boc-Cephalexin(28180-92-9)

Safety Data

• Hazardous Substances Data: 28180-92-9(Hazardous Substances Data)

Usage

Chemical Properties

Light Yellow Solid

Uses

Different sources of media describe the Uses of 28180-92-9 differently. You can refer to the following data:
1. N-Boc-Cephalexin is a protected Cephalexin (C256800), a semi-synthetic cephalosporin antibiotic.
2. Protected Cephalexin (C256800), a cephalosporin antibiotic.

Upstream product

• 59176-12-4 1ξ-oxo-6β-(2-phenyl-acetylamino)-1λ⁴-penicillanic acid (Ξ)-1-methoxycarbonyl-2-oxo-propyl ester 
• 59176-13-5 (6R)-3-methyl-8-oxo-7t-(2-phenyl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid (Ξ)-1-methoxycarbonyl-2-oxo-propyl ester 
• 57872-62-5 N-tert-butyloxycarbonylcefradine 
• 33125-05-2 Boc-D-Phg-OH 
• 875-74-1 (R)-phenylglycine 
• 31461-05-9 (6R)-3-methyl-8-oxo-7t-(trimethylsilanyl-amino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid trimethylsilanyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 15686-71-2 cefalexin 
• 66254-02-2 (6R)-7t-((R)-2-tert-butoxycarbonylamino-2-phenyl-acetylamino)-3-methyl-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid (Ξ)-1-methoxycarbonyl-2-oxo-propyl ester 

Downstream Products

• 79750-46-2 (6R,7R)-3-methyl-7-[(R)-2-amino-2-phenylacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid 

Relevant articles and documents

Synthesis and biochemical evaluation of cephalosporin analogues equipped with chemical tethers

Molecular probes typically require structural modifications to allow for the immobilisation or bioconjugation with a desired substrate but the effects of these changes are often not evaluated. Here, we set out to determine the effects of attaching functio

Synthesis of potential impurities of cefalexin and cefradine

The synthesis of some impurities of the cephalosporin antibiotics cefalexin and cefradine is described. These impurities which may be present in commercial samples are formed during the semi-synthetic preparation of these antibiotics or upon their degradation. The preparation of these compounds enables the validation of selective quantitative analytical methods, such as column liquid chromatography and thin layer chromatography.