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4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside is a complex organic compound that plays a significant role in organic synthesis. It is characterized by its unique structure, which includes a 4-nitrophenyl group, an acetamido group, and multiple sugar moieties, including a fucopyranosyl and two glucopyranosyl units. 4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside is known for its potential applications in various fields, particularly in the synthesis of biologically active molecules and the development of new pharmaceuticals.

93496-53-8

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93496-53-8 Usage

Uses

Used in Organic Synthesis:
4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside is used as a key intermediate in organic synthesis for the preparation of various biologically active compounds. Its unique structure allows for the formation of complex molecules with potential applications in the pharmaceutical industry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside is used as a building block for the development of new drugs. Its sugar moieties and other functional groups can be modified to create novel compounds with potential therapeutic properties.
Used in Research and Development:
4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside is also used in research and development for the study of its chemical properties and potential applications. Scientists can use 4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside to explore new synthetic routes and develop innovative methods for the synthesis of complex organic molecules.
Used in Analytical Chemistry:
In analytical chemistry, 4-Nitrophenyl2-acetamido-2-deoxy-3-O-[2-O-(a-L-fucopyranosyl)-b-D-galactopyranosyl]-b-D-glucopyranoside can be employed as a reference compound for the development and validation of analytical methods. Its unique structure and properties make it suitable for the calibration of instruments and the assessment of method performance.

Check Digit Verification of cas no

The CAS Registry Mumber 93496-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,9 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93496-53:
(7*9)+(6*3)+(5*4)+(4*9)+(3*6)+(2*5)+(1*3)=168
168 % 10 = 8
So 93496-53-8 is a valid CAS Registry Number.

93496-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl 2-acetamido-2-deoxy-3-O-(2-O-(α-L-fucopyranosyl)-β-D-glucopyranoside)-

1.2 Other means of identification

Product number -
Other names H type 1 β-NP Glycoside

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:93496-53-8 SDS

93496-53-8Downstream Products

93496-53-8Relevant academic research and scientific papers

SYNTHESIS OF SOME OLIGOSACCHARIDES CONTAINING THE O-α-L-FUCOPYRANOSYL-(1->2)-D-GALACTOPYRANOSYL UNIT

Matta, Khushi L.,Rana, Surjit S.,Piskorz, Conrad F.,Abbas, Saeed A.

, p. 247 - 256 (2007/10/02)

A practical approach for the synthesis of oligosaccharides containing the O-α-L-fucopyranosyl-(1->2)-D-galactopyranosyl unit has been developed by utilizing the readily accessible 3,4,6-tri-O-acetyl-2-O-(2,3,4-tri-O-acetyl-α-L-fucopyranosyl)-α-D-galactopy

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