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29776-43-0

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29776-43-0 Usage

Description

2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE is a white solid that serves as a valuable synthetic intermediate in the field of carbohydrate chemistry. Its unique structure allows for various chemical modifications, making it a versatile compound for research and development.

Uses

Used in Carbohydrate Chemistry:
2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE is used as a synthetic intermediate for the preparation of pure methyl aand b-glycosides of D-glucosamine. Its application in this field is crucial for the development of new carbohydrate-based compounds and their potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE can be utilized as a key building block for the synthesis of complex carbohydrate-based drugs. Its ability to form various derivatives makes it a promising candidate for the development of novel therapeutic agents.
Used in Research and Development:
2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE is also used in research and development for the study of carbohydrate structures and their interactions with biological systems. This knowledge can lead to a better understanding of various biological processes and the development of targeted therapies for various diseases.
Used in Material Science:
In material science, 2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE can be employed in the development of novel carbohydrate-based materials with unique properties. These materials could have potential applications in areas such as drug delivery, sensors, and biocompatible materials.

Check Digit Verification of cas no

The CAS Registry Mumber 29776-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,7 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29776-43:
(7*2)+(6*9)+(5*7)+(4*7)+(3*6)+(2*4)+(1*3)=160
160 % 10 = 0
So 29776-43-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H19NO6/c1-8(17)16-11-12(18)13-10(21-14(11)19)7-20-15(22-13)9-5-3-2-4-6-9/h2-6,10-15,18-19H,7H2,1H3,(H,16,17)/t10-,11-,12-,13-,14?,15?/m1/s1

29776-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-D-GLUCOPYRANOSE

1.2 Other means of identification

Product number -
Other names 2-Acetamido-4,6-O-benzyliden-2-desoxy-D-glucose

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:29776-43-0 SDS

29776-43-0Relevant articles and documents

Novel phosphoramidate prodrugs of N-acetyl-(d)-glucosamine with antidegenerative activity on bovine and human cartilage explants

Serpi, Michaela,Bibbo, Rita,Rat, Stephanie,Roberts, Helen,Hughes, Claire,Caterson, Bruce,Alcaraz, María José,Gibert, Anna Torrent,Verson, Carlos Raul Alaez,McGuigan, Christopher

supporting information; experimental part, p. 4629 - 4639 (2012/07/01)

(d)-Glucosamine and other nutritional supplements have emerged as safe alternative therapies for osteoarthritis (OA), a chronic and degenerative articular joint disease. In our preceding paper, a series of novel O-6 phosphate N-acetyl (d)-glucosamine prod

PROCESS FOR THE SYNTHESIS OF L-FUCOSYL DI- OR OLIGO-SACCHARIDES AND NOVEL 2,3,4 TRIBENZYL-FUCOSYL DERIVATIVES INTERMEDIATES THEREOF

-

Page/Page column 15, (2011/10/13)

The present invention relates to a process for the synthesis of L-fucosyl di- or oligosaccharides and their novel 2,3,4-tri-O-benzyl-fucosyl synthetic intermediates derivatives of easy crystallization. In particular the present invention relates to a proc

Substrate specificity of N-acetylhexosamine kinase towards N-acetylgalactosamine derivatives

Cai, Li,Guan, Wanyi,Wang, Wenjun,Zhao, Wei,Kitaoka, Motomitsu,Shen, Jie,O'Neil, Crystal,Wang, Peng George

supporting information; experimental part, p. 5433 - 5435 (2010/05/02)

We report herein a bacterial N-acetylhexosamine kinase, NahK, with broad substrate specificity towards structurally modified GalNAc analogues, and the production of a GalNAc-1-phosphate library using this kinase.

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