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2-Trichloromethyl-1,3-dioxolane, also known as chloral beta-dioxolane, is a chemical compound with the molecular formula C3H3Cl3O2. It is a colorless liquid with a pungent odor and is used as a chlorinating agent in organic synthesis. 2-Trichloromethyl-1,3-dioxolane is formed by the reaction of chloral with ethylene oxide and is known for its ability to introduce chlorine atoms into various organic molecules. It is also used as a solvent and a reagent in the pharmaceutical and chemical industries. Due to its reactivity and potential health risks, it is important to handle 2-Trichloromethyl-1,3-dioxolane with caution, following proper safety protocols.

5660-66-2

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5660-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5660-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5660-66:
(6*5)+(5*6)+(4*6)+(3*0)+(2*6)+(1*6)=102
102 % 10 = 2
So 5660-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H5Cl3O2/c5-4(6,7)3-8-1-2-9-3/h3H,1-2H2

5660-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trichloromethyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5660-66-2 SDS

5660-66-2Relevant academic research and scientific papers

2-Dichloromethyl-1,3-dioxolan-2-yl orthoesters. A potential protecting group for sugar derivatives

Oezgener,Yueceer

, p. 559 - 567 (2007/10/03)

Reactions of 2-dichloromethylene-1,3-dioxolane (2) with acetal protected sugar derivatives in neutral media gave 2-dichloromethyl-1,3-dioxolan-2-yl orthoesters. These orthoesters are readily hydrolysed under mild acidic conditions offering a new method for the preparation of readily removable protecting groups. This strategy was realised in the preparation of 6-O-acetyl-3,5-di-O-methyl-1,2-O-isopropylidene-α-D-glucofuranose.

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