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5207-08-9

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5207-08-9 Usage

Description

.beta.-D-Glucopyranose, 1,1-dithiobis1-deoxy-, octaacetate is a chemical compound derived from a glucose molecule with eight acetate groups attached. .beta.-D-Glucopyranose, 1,1-dithiobis1-deoxy-, octaacetate serves as a protecting group for carbohydrates in organic synthesis, providing stability to the glucose molecule and enabling various chemical reactions such as esterifications and acylations. It is also utilized in the preparation of glycosides and other carbohydrate derivatives, protecting hydroxyl groups in the glucose molecule. Furthermore, it is a valuable tool in carbohydrate chemistry research and the development of new pharmaceuticals and bioactive compounds.

Uses

Used in Organic Synthesis:
.beta.-D-Glucopyranose, 1,1-dithiobis1-deoxy-, octaacetate is used as a protecting group for carbohydrates in organic synthesis to facilitate various chemical reactions, such as esterifications and acylations. The protection of hydroxyl groups in the glucose molecule allows for selective reactions and prevents unwanted side reactions.
Used in Pharmaceutical Development:
.beta.-D-Glucopyranose, 1,1-dithiobis1-deoxy-, octaacetate is used as a valuable tool in the study of carbohydrate chemistry and the development of new pharmaceuticals and bioactive compounds. Its ability to protect hydroxyl groups in the glucose molecule makes it an essential component in the synthesis of complex carbohydrate-based drugs and therapies.
Used in Preparation of Glycosides:
.beta.-D-Glucopyranose, 1,1-dithiobis1-deoxy-, octaacetate is used in the preparation of glycosides and other carbohydrate derivatives. The octaacetate derivative provides stability to the glucose molecule, allowing for the formation of glycosidic bonds and the creation of a diverse range of carbohydrate-based compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5207-08-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5207-08:
(6*5)+(5*2)+(4*0)+(3*7)+(2*0)+(1*8)=69
69 % 10 = 9
So 5207-08-9 is a valid CAS Registry Number.

5207-08-9SDS

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 bis(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)disulfide

1.2 Other means of identification

Product number -
Other names bis(2,3,4,6-tetra-O-acetyl-1-thio-b-D-glucopyranosyl)1,1'-disulfide

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:5207-08-9 SDS

5207-08-9Relevant articles and documents

Controllable Activation of Pd-G3 Palladacycle Precatalyst in the Presence of Thiosugars: Rapid Access to 1-Aminobiphenyl Thioglycoside Atropoisomers at Room Temperature

AL-Shuaeeb, Riyadh Ahmed Atto,Dejean, Camille,Alami, Mouad,Messaoudi, Samir

supporting information, p. 3114 - 3118 (2017/12/26)

A controllable method for the functionalization of XantPhos Pd-G3 precatalyst with thiosugars and thiols has been established. Under mild and operationally simple reaction conditions through just mixing of precatalyst and thiosugars (α- or β-mono-, di- and poly-thiosugar derivatives) in water at 25 °C for 20 min, a series of 1-aminobiphenyl thioglycosides that are difficult to synthesize by classical methods has been synthesized in very high yields.

Free-radical hydrothiolation of glycals: A thiol-ene-based synthesis of S-disaccharides

Staderini, Samuele,Chambery, Angela,Marra, Alberto,Dondoni, Alessandro

supporting information; experimental part, p. 702 - 704 (2012/02/15)

A method for the synthesis of a new family of 1-deoxy S-disaccharides has been established via free-radical hydrothiolation of glycals by sugar thiols (thiol-ene coupling). The photoinduced coupling between four tri-O-acetyl-d-glycals and three different sugar thiols reveals that the reaction efficiency and stereoselectivity are highly dependent on the stereochemistry of the OAc groups at C3 and C4 of the glycal.

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