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65556-30-1

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65556-30-1 Usage

Description

1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose (CAS# 65556-30-1) is a white crystalline solid that serves as a valuable compound in the field of organic synthesis. Its unique structure and properties make it a versatile building block for the development of various complex organic molecules and pharmaceuticals.

Uses

Used in Organic Synthesis:
1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose is used as a synthetic intermediate for the creation of complex organic molecules. Its structural features allow for the formation of various derivatives, which can be further utilized in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose is used as a key building block for the development of novel drug candidates. Its unique structure can be exploited to design and synthesize new molecules with potential therapeutic applications, targeting a wide range of diseases and medical conditions.
Used in Research and Development:
In the field of research and development, 1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose serves as an important compound for studying the synthesis and properties of complex carbohydrates and their derivatives. It can also be used to investigate the interactions of these molecules with biological systems, providing valuable insights into their potential applications in medicine and other fields.
Used in Material Science:
1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose can be employed in the development of advanced materials, such as polymers and coatings, with unique properties. Its incorporation into these materials can lead to enhanced performance characteristics, such as improved stability, biocompatibility, or specific interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 65556-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,5 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65556-30:
(7*6)+(6*5)+(5*5)+(4*5)+(3*6)+(2*3)+(1*0)=141
141 % 10 = 1
So 65556-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C31H34O8/c1-22(32)34-21-27-28(35-18-24-12-6-3-7-13-24)29(36-19-25-14-8-4-9-15-25)30(31(39-27)38-23(2)33)37-20-26-16-10-5-11-17-26/h3-17,27-31H,18-21H2,1-2H3

65556-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose

1.2 Other means of identification

Product number -
Other names 6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranosyl acetate

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:65556-30-1 SDS

65556-30-1Downstream Products

65556-30-1Relevant articles and documents

2-Diphenylphosphinonyl-acetyl as a Remote Directing Group for the Highly Stereoselective Synthesis of β-Glycosides

Liu, Xianglai,Lin, Yetong,Liu, Ao,Sun, Qianhui,Sun, Huiyong,Xu, Peng,Li, Guolong,Song, Yingying,Xie, Weijia,Sun, Haopeng,Yu, Biao,Li, Wei

supporting information, p. 443 - 452 (2021/12/27)

The configuration of the anomeric glycosidic linkages is crucial for maintaining the biological functions and activities of carbohydrate molecules. However, their stereochemistry control in glycosylation represents one of the most challenging tasks in car

Four Different Regioisomeric Polycarbonates Derived from One Natural Product, d -Glucose

Lonnecker, Alexander T.,Lim, Young H.,Felder, Simcha E.,Besset, Céline J.,Wooley, Karen L.

, p. 7857 - 7867 (2016/11/09)

Strategies for the preparation of polycarbonates, derived from the natural product d-glucose, which have the potential to degrade back into their bioresorbable starting material and CO2, were developed. By employing established carbohydrate pro

A novel selectfluor-mediated regioselective O-benzyl ether acetolysis of perbenzylated monosaccharides

Tambie, Marlon S.,Jalsa, Nigel Kevin

, p. 545 - 559 (2016/04/19)

Selectfluor, a source of the super electrophile F+, has replaced conventional reagents that supply F+ for fluorination due to its attractive physical and chemical properties. This study is the first report of using Selectfluor as a d

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