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57467-13-7

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  • 4-Nitrophenyl 2-acetamido-2-deoxy-3-O-(-β-D-galactopyranosyl)-β-D-glucopyranoside 57467-13-7

    Cas No: 57467-13-7

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57467-13-7 Usage

Description

BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P, also known as p-Nitrophenyl 2-Acetamido-2-deoxy-3-O-(β-D-galactopyranosyl)-β-D-glucopyranoside, is a complex carbohydrate derivative with a chemical structure consisting of a β-D-galactopyranosyl linked to a β-D-glucopyranoside, which is further connected to a p-nitrophenyl group. BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P is characterized by its white solid appearance and is primarily used in organic synthesis.

Uses

1. Organic Synthesis:
BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P is used as a synthetic building block for the creation of various complex carbohydrates and glycoconjugates. Its unique structure allows for the development of novel compounds with potential applications in various fields, such as pharmaceuticals, biotechnology, and materials science.
2. Pharmaceutical Applications:
In the pharmaceutical industry, BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can be used as a key intermediate in the synthesis of glycoconjugate drugs, which have the potential to target specific biological receptors and modulate cellular processes. These drugs can be employed for the treatment of various diseases, including cancer, inflammatory disorders, and infectious diseases.
3. Biotechnology Applications:
In the biotechnology sector, BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can be utilized in the development of glyco-engineered proteins and enzymes. These glyco-engineered biomolecules can exhibit improved stability, solubility, and bioactivity, making them valuable tools for research and therapeutic applications.
4. Materials Science Applications:
BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can also be employed in the field of materials science for the design and synthesis of carbohydrate-based materials, such as hydrogels, nanoparticles, and self-assembled structures. These materials can find applications in drug delivery, tissue engineering, and sensing technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 57467-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,6 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57467-13:
(7*5)+(6*7)+(5*4)+(4*6)+(3*7)+(2*1)+(1*3)=147
147 % 10 = 7
So 57467-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H28N2O13/c1-8(25)21-13-18(35-20-17(29)16(28)14(26)11(6-23)34-20)15(27)12(7-24)33-19(13)32-10-4-2-9(3-5-10)22(30)31/h2-5,11-20,23-24,26-29H,6-7H2,1H3,(H,21,25)

57467-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl 2-acetamido-2-deoxy-3-O-(b-D-galactopyranosyl)-b-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names p-nitrophenyllacto-N-biose

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:57467-13-7 SDS

57467-13-7Relevant articles and documents

Facile preparation of indoxyl- and nitrophenyl glycosides of lactosamine and isolactosamine

Boettcher, Stephan,Thiem, Joachim

, p. 10856 - 10861 (2014/03/21)

The synthesis of the novel indoxyl glycosides of N-acetyl-lactosamine (X-LacNAc) and N-acetyl-isolactosamine (X-LNB) is reported employing glycosyl chlorides in a facile phase transfer glycosylation, followed by mild decarboxylation and finally deacetylat

Enhanced enzymatic reactions in a microchannel reactor

Kanno, Kenichi,Kawazumi, Hirofumi,Miyazaki, Masaya,Maeda, Hideaki,Fujii, Masayuki

, p. 687 - 690 (2007/10/03)

Organic and enzymatic reactions in microchannel reactors were discussed. Hydrolytic activity of a microchannel pre-treated with enzyme solution was studied. It was found that the reaction rate in microchannel is much faster than the micro test tube. Mass transfer is also much more efficient in microchannel.

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