2862-03-5

Basic information

• Product Name: 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID
• Synonyms: 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID;ALPHA-BENZYL-4,6-O-BENZYLIDENE-MURAMIC ACID;BENZYL 2-ACETAMIDO-4,6-O-BENZYLIDENE-3-O-[1-(R)-CARBOXYETHYL]-2-DEOXY-A-D-GLUCOPYRANOSE;Benzyl N-Acetyl-4,6-O-benzylidene-α-D-muramic Acid;(2R)-{[(4aR,6S,7R,8R,8aS)-7-(Acetylamino)-6-(benzyloxy)-2-phenylperhydropyrano[3,2-d][1,3]dioxin-8-yl]oxy}propanoic acid, N-Acetyl-1-O-(phenylmethyl)-4,6-O-(phenylmethylene-alpha-muramic acid;2-(3-Acetamido-2-benzyl-4,6,O-benzylidene-alpha-D-glucopyranosid-4-yloxy)propanoic acid tech;Benzyl 2-AcetaMido-4,6-O-benzylidene-3-O-(D-1-carboxyethyl)-2-deoxy-glucopyranoside;N-Acetyl-1-O-(phenylMethyl)-4,6-O-(phenylMethylene)-α-MuraMic Acid
• CAS NO: 2862-03-5
• Molecular Formula: C₂₅H₂₉NO₈
• Molecular Weight: 471.49966
• Product Categories: Carbohydrates & Derivatives
• Mol File: 2862-03-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 237-239° C
• Appearance: /
• Storage Temp.: -20?C Freezer
• Solubility: DMSO, Methanol
• Stability: Store at 2-8°C
• CAS DataBase Reference: 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID(2862-03-5)
• EPA Substance Registry System: 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID(2862-03-5)

Safety Data

• Hazardous Substances Data: 2862-03-5(Hazardous Substances Data)

Usage

Description

2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID is a complex organic compound with a unique chemical structure. It is a benzyl derivative of muramic acid, which is an amino sugar that is a key component of peptidoglycan, the main skeletal structure of bacterial cell walls in both Gram-positive and Gram-negative bacteria. 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID is characterized by its white solid appearance.

Uses

Used in Pharmaceutical Industry:
2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID is used as a pharmaceutical compound for its potential antibacterial properties. Due to its structural similarity to muramic acid, it may interfere with the synthesis of peptidoglycan in bacterial cell walls, thereby inhibiting bacterial growth and functioning as an antimicrobial agent.
Used in Research and Development:
In the field of research and development, 2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID serves as a valuable compound for studying the structure and function of bacterial cell walls. It can be used to develop new antibiotics or to understand the mechanisms of bacterial resistance to existing antibiotics.
Used in Chemical Synthesis:
2-(3-ACETAMIDO-2-BENZYL-4,6,OBENZYLIDENE-ALPHA-D-GLUCOPYRNOSID-4-YLOXY)PROPIONIC ACID can also be utilized as a building block or intermediate in the synthesis of more complex organic molecules, particularly those with potential applications in the pharmaceutical, agrochemical, or materials science industries. Its unique structure and functional groups make it a versatile starting material for various chemical reactions and modifications.

Upstream product

• 104371-51-9 Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-<(R)-1-(methoxycarbonyl)ethyl>-α-D-glucopyranoside 
• 13343-62-9 benzyl 2-acetamido-2-deoxy-α-D-glucopyranoside 
• 100-51-6 benzyl alcohol 
• 74533-11-2 L-2-chloropropionic acid sodium salt 
• 13343-63-0 benzyl 4,6-O-benzylidene-2-acetylamino-2-deoxy-α-D-glucopyranoside 
• 535-11-5 Ethyl 2-bromopropionate 
• 29617-66-1 (S)-2-chloropropanoic acid 
• 7512-17-6 N-Acetyl-D-glucosamine 

Downstream Products

• 104371-51-9 Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-<(R)-1-(methoxycarbonyl)ethyl>-α-D-glucopyranoside 
• 129145-18-2 (R)-2-{(S)-2-[(R)-2-((4aR,6S,7R,8R,8aS)-7-Acetylamino-6-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionylamino]-propionylamino}-pentanedioic acid 1-amide 5-dibutylamide 
• 129145-17-1 (R)-2-{(S)-2-[(R)-2-((4aR,6S,7R,8R,8aS)-7-Acetylamino-6-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionylamino]-propionylamino}-pentanedioic acid 1-amide 5-dodecylamide 
• 63092-13-7 1-O-benzyl-4,6-O-benzylidene-N-acetylmuramyl-alanyl-D-glutamic acid diamide 
• 124453-32-3 1-α-O-benzyl-4,6-O-benzylidene-N-acetylmuramyl-L-α-aminobutyryl-D-glutamine n-butyl ester 
• 76502-94-8 1-O-benzyl-4,6-O-benzylidene-N-acetylmuramyl-alanyl-D-isoglutamine methyl ester 
• 95900-15-5 N-<2-O-(benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside-3-yl)-(R)-lactoyl>-L-alanylglycine methyl ester 
• 171669-19-5 (R)-2-{(S)-2-[(R)-2-((4aR,6S,7R,8R,8aS)-7-Acetylamino-6-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionylamino]-propionylamino}-pentanedioic acid 1-amide 5-[(6-azido-hexyl)-amide] 
• 171669-20-8 benzyl 6-hexanoate 
• 72009-73-5 Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-<(R)-1-carboxyethyl>-α-D-glucopyranoside, HONB ester 
• 35477-96-4 O¹-benzyl-O⁴,O⁶-(R)-benzylidene-β-muramic acid lactam 
• 35477-92-0 O¹-benzyl-O⁴,O⁶-diacetyl-β-muramic acid lactam 
• 35477-97-5 O¹-benzyl-β-muramic acid lactam 
• 35478-00-3 O¹-benzyl-O⁴-acetyl-O⁶-trityl-β-muramic acid lactam 

Relevant articles and documents

The synthesis and biological activities of anomeric butyl glycosides of muramyl dipeptide

The synthesis of anomeric butyl glycosides of muramyl dipeptide was reported. α-Butyl glycoside of N-acetyl-D-glucosamine was 3-O-benzylidenated and the benzylidene derivative was 3-O-alkylated by the Williamson reaction with sodium (S)-2-chloropropionate

Muramyl peptides. I. Stereochemically pure derivatives of muramic and isomuramic acids

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