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NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER is a complex chemical compound that features a unique structure consisting of N-acetylglucosamine, asparagine, and benzyl ester. NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER is pivotal in the field of organic synthesis and research, especially within the realm of carbohydrate chemistry. Its intricate composition renders it an indispensable building block for the synthesis of oligosaccharides and glycoconjugates, making it a valuable asset for chemists and biochemists delving into the intricate roles carbohydrates play in biological processes.

219968-28-2

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219968-28-2 Usage

Uses

Used in Organic Synthesis:
NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER is used as a key building block for the synthesis of complex oligosaccharides and glycoconjugates, which are essential in various biological processes.
Used in Carbohydrate Chemistry Research:
In the field of carbohydrate chemistry, NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER serves as a crucial tool for chemists and biochemists to study the structure, function, and interactions of carbohydrates in biological systems.
Used in Pharmaceutical Industry:
NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER is used as a precursor in the development of pharmaceutical compounds, particularly those targeting carbohydrate-based drug discovery.
Used in Biochemical Research:
NOMEGA-(2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-NALPHA-(TERT-BUTOXYCARBONYL)-L-ASPARAGINE BENZYL ESTER is utilized in biochemical research to understand the role of carbohydrates in cell recognition, signaling, and other biological activities, contributing to the advancement of glycobiology.

Check Digit Verification of cas no

The CAS Registry Mumber 219968-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,9,6 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219968-28:
(8*2)+(7*1)+(6*9)+(5*9)+(4*6)+(3*8)+(2*2)+(1*8)=182
182 % 10 = 2
So 219968-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C45H53N3O10/c1-31(49)46-39-41(55-28-34-21-13-7-14-22-34)40(54-27-33-19-11-6-12-20-33)37(30-53-26-32-17-9-5-10-18-32)57-42(39)48-38(50)25-36(47-44(52)58-45(2,3)4)43(51)56-29-35-23-15-8-16-24-35/h5-24,36-37,39-42H,25-30H2,1-4H3,(H,46,49)(H,47,52)(H,48,50)/t36-,37+,39+,40+,41+,42+/m0/s1

219968-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (2S)-4-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]amino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoate

1.2 Other means of identification

Product number -
Other names -(2-Acetamido-3,4,6-tri--benzyl-2-deoxy-β--glucopyranosyl)--Boc--asparagine Benzyl Ester

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:219968-28-2 SDS

219968-28-2Downstream Products

219968-28-2Relevant academic research and scientific papers

A simple method for the synthesis of N(β)-glycosylated-asparagine and - glutamine derivatives

Mizuno, Mamoru,Muramoto, Ikuyo,Kobayashi, Katsuaki,Yaginuma, Hiroshi,Inazu, Toshiyuki

, p. 162 - 165 (2007/10/03)

N(β)-Glycosylated-asparagine and -glutamine derivatives, which are useful precursors for the synthesis of N-glycopeptides and their analogs, were obtained in good yields by the reaction of a glycosyl azide and an N(α)-protected-aspartic/glutamic acid α-mo

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