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1,2:5,6-DI-O-ISOPROPYLIDENE-3-O-(2-THIAPROPYL)-ALPHA-D-GLUCOFURANOSE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21665-19-0

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21665-19-0 Usage

Sugar derivative

Contains a furanose ring
The compound is derived from a sugar (glucose) and features a furanose ring, which is a five-membered ring structure commonly found in carbohydrates.

Isopropylidene groups

Two isopropylidene groups are attached to the sugar ring
These groups are used to protect specific hydroxyl (-OH) functionalities in the molecule, preventing unwanted reactions at those sites.

Thiapropyl group

One thiapropyl group is attached to the sugar ring
This group is a sulfur-containing analog of a propyl group, which is also used as a protecting group for hydroxyl functionalities.

Protecting group

Commonly employed as a protecting group in carbohydrate chemistry
The compound serves as a temporary shield for hydroxyl groups, allowing for selective modification of the sugar molecule without affecting the protected sites.

Applications

Used in organic synthesis and carbohydrate biochemistry research
The compound is of interest in both organic chemistry and biochemistry, particularly in the study of carbohydrates and their interactions with other molecules.

Stereochemistry

alpha-D-glucopyranose
The compound has a specific stereochemistry, with the hydroxyl group at the C1 position being in the alpha configuration, and the sugar ring being in the pyranose form (a six-membered ring).

Solubility

Not explicitly mentioned in the material, but as a sugar derivative, it is likely soluble in polar solvents such as water and methanol.

Stability

The compound is stable under normal laboratory conditions, but it may be sensitive to acidic or basic conditions that could potentially remove the protecting groups.

Reactivity

The compound is relatively unreactive due to the presence of protecting groups, but it can undergo specific reactions to modify the sugar molecule at unshielded sites.

Check Digit Verification of cas no

The CAS Registry Mumber 21665-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,6 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21665-19:
(7*2)+(6*1)+(5*6)+(4*6)+(3*5)+(2*1)+(1*9)=100
100 % 10 = 0
So 21665-19-0 is a valid CAS Registry Number.

21665-19-0SDS

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 (3aR,5R,6S,6aR)-5-[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]-2,2-dimet hyl-6-[(methylsulfanyl)methoxy]tetrahydrofuro[2,3-d][1,3]dioxole (non-preferred name)

1.2 Other means of identification

Product number -
Other names 1,2:13,14-Diepoxytetradecane

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:21665-19-0 SDS

21665-19-0Downstream Products

21665-19-0Relevant academic research and scientific papers

Glycosylated vinyl ethers by the Julia-Lythgoe-Kocienski olefination: application to the synthesis of 2′,5′-dideoxydisaccharides and carbohydrated β-lactams

Sanchez, Ivan Perez,Turos, Edward

experimental part, p. 1646 - 1660 (2009/12/04)

α-Carbohydrated pyridinyl sulfones, prepared from commercially available d-(-)-ribose, d-(+)-galactose, and d-(+)-glucose through a five-step sequence, have been employed in the Julia-Lythgoe-Kocienski olefination with aldehydes. This one-pot protocol, us

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