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2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE, also known as 2,3,4,6-Tetra-O-benzyl-D-mannopyranose (CAS# 61330-61-8), is a synthetic carbohydrate derivative with a unique structure. It is characterized by the presence of four benzyl groups attached to the hydroxyl groups of the alpha-D-mannopyranose molecule, which provides it with specific chemical and physical properties. 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE is a versatile intermediate in organic synthesis and has potential applications in various fields.

61330-61-8

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61330-61-8 Usage

Uses

Used in Organic Synthesis:
2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE is used as a synthetic intermediate for the preparation of various complex carbohydrate structures and derivatives. Its benzyl-protected hydroxyl groups allow for selective reactions and modifications, making it a valuable building block in the synthesis of bioactive compounds, pharmaceuticals, and other organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE is used as a key component in the development of glycoconjugate drugs and vaccines. Its ability to mimic natural glycans and interact with biological systems makes it a promising candidate for the design of new therapeutic agents targeting specific receptors and pathways.
Used in Chemical Research:
2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE is also utilized in chemical research for studying the properties and reactivity of carbohydrates. Its unique structure allows researchers to investigate the influence of benzyl protection on the chemical behavior of sugar molecules, providing insights into the development of new synthetic methods and strategies.
Used in Material Science:
In the field of material science, 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSE can be employed as a functional component in the design of advanced materials with specific properties. Its ability to form hydrogen bonds and interact with other molecules can contribute to the development of new materials with applications in sensors, drug delivery systems, and other areas.

Check Digit Verification of cas no

The CAS Registry Mumber 61330-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,3 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61330-61:
(7*6)+(6*1)+(5*3)+(4*3)+(3*0)+(2*6)+(1*1)=88
88 % 10 = 8
So 61330-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C34H36O6/c35-34-33(39-24-29-19-11-4-12-20-29)32(38-23-28-17-9-3-10-18-28)31(37-22-27-15-7-2-8-16-27)30(40-34)25-36-21-26-13-5-1-6-14-26/h1-20,30-35H,21-25H2/t30-,31-,32+,33+,34+/m1/s1

61330-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,5R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-ol

1.2 Other means of identification

Product number -
Other names 2,3,4,6-Tetra-O-benzyl-D-mannose

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:61330-61-8 SDS

61330-61-8Relevant academic research and scientific papers

IMPROVED PROCESS FOR PREPARATION OF 2,3,4,6-TETRA-O-BENZYL-D-GALACTOSE

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Page/Page column 25; 26; 27; 28, (2020/01/08)

Provided herein is an improved process for the preparation of benzylated derivative of D-galactose, particularly 2,3,4,6-tetra-O-benzyl-D-galactose that gives higher yield and better purity being cost effective with reduced impurities.

Derivatives of hydrazino-monosaccharides and aldohexoses which are useful as intermediates for preparing compounds or as compounds which lower the uric acid

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, (2008/06/13)

Substituted hydrazino- and pyrazolo-aldopentoses and aldohexoses, which are useful as intermediates for preparing compounds, as compounds which lower the uric acid level in the blood, and as bactericides, are provided. The substituted hydrazino compounds also enter into chemical reactions which are not possible with their unsubstituted counterparts.

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