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14419-59-1

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14419-59-1 Usage

Description

P-AMINOPHENYL-2-ACETAMIDO-2-DEOXY-B-D-GL UCOPYRANOS is a derivative of N-acetylglucosamine, which is a determinant group in artificial antigens. It is a tan solid with unique chemical properties that make it suitable for various applications.

Uses

Used in Pharmaceutical Industry:
P-AMINOPHENYL-2-ACETAMIDO-2-DEOXY-B-D-GL UCOPYRANOS is used as a pharmaceutical compound for its role in the development of artificial antigens. Its N-acetylglucosamine derivative nature allows it to be a key component in the creation of antigens that can be used for various medical and therapeutic purposes.
Used in Research and Development:
In the field of research and development, P-AMINOPHENYL-2-ACETAMIDO-2-DEOXY-B-D-GL UCOPYRANOS is used as a chemical compound for studying the properties and interactions of N-acetylglucosamine derivatives. This helps in understanding their potential applications in various industries, including pharmaceuticals, biotechnology, and material science.
Used in Material Science:
P-AMINOPHENYL-2-ACETAMIDO-2-DEOXY-B-D-GL UCOPYRANOS is also used in material science as a component in the development of new materials with specific properties. Its unique chemical structure and tan solid form can contribute to the creation of materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 14419-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,1 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14419-59:
(7*1)+(6*4)+(5*4)+(4*1)+(3*9)+(2*5)+(1*9)=101
101 % 10 = 1
So 14419-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O6/c1-7(18)16-11-13(20)12(19)10(6-17)22-14(11)21-9-4-2-8(15)3-5-9/h2-5,10-14,17,19-20H,6,15H2,1H3,(H,16,18)/t10?,11-,12+,13+,14+/m0/s1

14419-59-1SDS

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 P-AMINOPHENYL-2-ACETAMIDO-2-DEOXY-B-D-GL UCOPYRANOS

1.2 Other means of identification

Product number -
Other names 4-Aminophenyl 2-Acetamido-2-deoxy--D-glucopyranoside

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:14419-59-1 SDS

14419-59-1Relevant articles and documents

Synthesis and biodistribution studies of carbohydrate derivatives radiolabeled with technetium-99m

de Barros, Andre Luis Branco,Cardoso, Valbert Nascimento,Mota, Luciene das Gracas,Alves, Ricardo Jose

scheme or table, p. 315 - 317 (2010/04/05)

Three carbohydrate derivatives, MAG3-Gl, MAG3-Ga, MAG3-NG, were synthesized and radiolabeled in high yields. These substances were injected in health Swiss mice and their biodistribution were evaluated. Among them, 99

Synthesis of 4-aminophenyl N-acetyl-β-D-glucosaminide derivatives and their application to the rate-assay of N-acetyl-β-D-glucosaminidase

Kasai,Okada,Yamaji

, p. 266 - 270 (2007/10/02)

Four N-acetyl-β-D-glucosaminides, 4-amino-2,6-dibromophenyl (1a), 4-amino-2,6-dichlorophenyl (1b), 4-amino-2-chlorophenyl (1c) and 4-aminophenyl N-acetyl-β-D-glucosaminides (1d) were synthesized. Substrates lac were hydrolyzed by N-acetyl-β-D-glucosaminid

Syntheses and Transformations of Glycohydrolase Substrates into Protein Conjugates Based on Michael Additions

Roy, Rene,Tropper, Francois D.,Morrison, Tara,Boratynski, Janusz

, p. 536 - 538 (2007/10/02)

The glycosyl chloride 1 and bromides 2 and 3 were stereospecifically transformed into p-nitrophenyl glycosides by phase transfer catalysis; these glycohydrolase substrates were reduced and N-acryloylated to afford Michael acceptors which reacted with amine functions of proteins.

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