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2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is a complex organic chemical compound characterized by the presence of a nitrophenyl group, an acetamido group, and three acetyl groups attached to a 2-deoxy-a-D-glucopyranoside molecule. 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is known for its potential biological activity and structural versatility, which makes it a valuable asset in organic synthesis and pharmaceutical research.

210418-02-3

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210418-02-3 Usage

Uses

Used in Pharmaceutical Research:
2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is used as a key intermediate in the synthesis of new drugs due to its unique structural features and potential biological activity. The presence of the nitrophenyl group may enhance the compound's reactivity, while the acetamido and acetyl groups can be utilized to modify its solubility and pharmacokinetics, thus improving its therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside serves as a versatile building block for the creation of various complex organic molecules. Its structural components can be manipulated to form a wide range of derivatives, making it a valuable tool for the development of novel chemical entities.
Used in Carbohydrate Chemistry:
2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is employed in the study of carbohydrate chemistry, where it can be used to explore the interactions between carbohydrates and other biomolecules. Its unique structure allows researchers to investigate the role of specific functional groups in carbohydrate recognition and binding.
Used in Glycosidase Mechanism Studies:
In the study of glycosidase mechanisms, 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside can be utilized as a substrate to understand the enzymatic processes involved in carbohydrate cleavage. Its structural features provide insights into the catalytic mechanisms of glycosidases and their substrate specificity.
Further research is required to fully comprehend the properties and potential applications of 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside, as its complex structure and diverse functional groups offer numerous opportunities for exploration in various scientific disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 210418-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,4,1 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 210418-02:
(8*2)+(7*1)+(6*0)+(5*4)+(4*1)+(3*8)+(2*0)+(1*2)=73
73 % 10 = 3
So 210418-02-3 is a valid CAS Registry Number.

210418-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-O-(4-Nitrophenyl)-α-D-N-acetylneuraminic acid ammonium salt

1.2 Other means of identification

Product number -
Other names -

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

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More Details:210418-02-3 SDS

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