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1000890-36-7

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1000890-36-7 Usage

Description

2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid, with the CAS number 1000890-36-7, is a pale yellow solid compound that plays a significant role in organic synthesis. It is a derivative of neuraminic acid, a key component of various biological molecules, and has unique chemical properties that make it valuable in the synthesis of complex organic compounds.

Uses

Used in Organic Synthesis:
2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid is used as a key intermediate in the synthesis of complex organic compounds. Its unique chemical properties allow for the formation of various derivatives and analogs, which can be further utilized in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid is used as a building block for the development of novel drug candidates. Its ability to form various derivatives makes it a versatile component in the design and synthesis of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid is also used in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its unique chemical properties enable the development of innovative compounds with improved efficacy and selectivity.
Used in Research and Development:
In the field of research and development, 2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid serves as a valuable tool for studying the structure and function of various biological molecules. Its unique properties allow researchers to probe the interactions between different biomolecules and gain insights into their mechanisms of action.
Overall, 2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid is a versatile compound with a wide range of applications across various industries, including organic synthesis, pharmaceuticals, agrochemicals, and research and development. Its unique chemical properties and potential for further modification make it an essential component in the development of innovative products and solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 1000890-36-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,8,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1000890-36:
(9*1)+(8*0)+(7*0)+(6*0)+(5*8)+(4*9)+(3*0)+(2*3)+(1*6)=97
97 % 10 = 7
So 1000890-36-7 is a valid CAS Registry Number.

1000890-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-O-(p-Nitrophenyl)-α-D-N-glycolylneuraminic Acid

1.2 Other means of identification

Product number -
Other names (2S,4S,5R,6R)-4-hydroxy-5-[(2-hydroxyacetyl)amino]-2-(4-nitrophenoxy)-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

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:1000890-36-7 SDS

1000890-36-7Upstream product

1000890-36-7Relevant articles and documents

Transsialidase from Trypanosoma cruzi for regio- and stereoselective synthesis of N-acyl-modified sialylated oligosaccharides and measurement of transfer rates

Schroven, Andreas,Meinke, Sebastian,Ziegelmueller, Patrick,Thiem, Joachim

, p. 9012 - 9021 (2008/09/16)

Recombinant transsialidase from Trypanosoma cruzi (TcTS) was used for the sialylation with natural and non-natural derivatives of neuraminic acid. Neu5Ac-α(2→3)-Gal-β(1→6)-Glc-αOMe was prepared in 80% yield. Correspondingly, the modified trisaccharide derivatives Neu5Prop-α(2 →3)-Gal-β(1 →6)-GlcαOMe (32%) and Neu5Gc-α(2→3)-Gal-β(1→6)-Glc-αOMe (Prop = propanoyl, Gc = glycolyl) were obtained in 60 % yield, respectively.

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