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74842-55-0

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74842-55-0 Usage

Description

BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID is a benzyl derivative of muramic acid, which is an amino sugar that plays a crucial role in the formation of peptidoglycan, the primary structural component of bacterial cell walls in both Gram-positive and Gram-negative bacteria. This white crystalline solid is known for its chemical properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID is used as a key component in the development of antibiotics for targeting bacterial cell walls. Its presence in peptidoglycan makes it a promising candidate for the creation of drugs that can disrupt bacterial cell wall synthesis, leading to the inhibition of bacterial growth and ultimately, the eradication of infections.
Used in Research and Development:
In the field of microbiology and biochemistry, BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID serves as an essential compound for research purposes. It is used to study the structure, function, and biosynthesis of peptidoglycan, which is vital for understanding bacterial cell wall assembly and the development of novel antimicrobial agents.
Used in Drug Design and Synthesis:
BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID is utilized as a building block in the design and synthesis of new drugs targeting bacterial infections. Its unique structure allows for the development of innovative molecules with enhanced antibacterial properties, potentially leading to the creation of more effective treatments for various bacterial diseases.
Used in Diagnostic Applications:
BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID can also be employed in the development of diagnostic tools and tests for the detection and identification of bacterial infections. By targeting the specific components of bacterial cell walls, such as peptidoglycan, these diagnostic tools can provide accurate and rapid identification of the causative agents, enabling timely and effective treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 74842-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74842-55:
(7*7)+(6*4)+(5*8)+(4*4)+(3*2)+(2*5)+(1*5)=150
150 % 10 = 0
So 74842-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C25H29NO8/c1-15(23(28)29)32-22-20(26-16(2)27)25(30-13-17-9-5-3-6-10-17)33-19-14-31-24(34-21(19)22)18-11-7-4-8-12-18/h3-12,15,19-22,24-25H,13-14H2,1-2H3,(H,26,27)(H,28,29)/t15?,19-,20-,21-,22-,24?,25+/m1/s1

74842-55-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BENZYL N-ACETYL-4,6-O-BENZYLIDENEMURAMIC ACID

1.2 Other means of identification

Product number -
Other names BENZYL N-ACETYL-4,6-O-BENZYLIDENE-A-D-MURAMIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74842-55-0 SDS

74842-55-0Relevant articles and documents

Optimization of UDP-N-acetylmuramic acid synthesis

Humljan, Jan,Starcevic,Car,Stefanic Anderluh,Kocjan,Jenko,Urleb

, p. 102 - 106 (2008/09/21)

UDP-N-acetylmuramic acid (UDP-MurNAc) is a substrate of MurC, an important enzyme in the intracellular pathway of bacterial peptidoglycan biosynthesis. Various approaches towards preparation of UDP-Mur/VAc have been published but these synthetic preparations were shown to include many problematic steps. An optimization study with the focus on muramyl phosphate and UMP-morpholidate coupling was performed, resulting in a synthetic procedure enabling robust and easily reproducible production on a multi-gram scale.

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