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89602-82-4

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89602-82-4 Usage

Structure

Five-membered ring containing oxygen and sulfur atoms
The dioxolane ring consists of two oxygen atoms and three carbon atoms, with a sulfur atom replacing one of the oxygen atoms.

Chloromethyl functional group

Attached to the 4-position of the dioxolane ring
The chloromethyl group (-CH2Cl) is connected to the fourth carbon atom in the ring.
4. Sulfur-containing heterocyclic compound
The compound has a heterocyclic ring structure with sulfur as one of the heteroatoms.

Potential applications

Organic synthesis, pharmaceuticals, and chemical production
The compound can be used as a building block or intermediate in the synthesis of various organic compounds, including pharmaceuticals and other chemicals.

Toxicity and environmental impact

Handle with caution
Due to its potential toxic or harmful effects on human health and the environment, it is important to use and handle 1,3-Dioxolane-2-thione, 4-(chloromethyl)carefully and follow safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 89602-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89602-82:
(7*8)+(6*9)+(5*6)+(4*0)+(3*2)+(2*8)+(1*2)=164
164 % 10 = 4
So 89602-82-4 is a valid CAS Registry Number.

89602-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(chloromethyl)-1,3-dioxolane-2-thione

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89602-82-4 SDS

89602-82-4Relevant articles and documents

Constructing the OCF2O moiety using BrF3

Hagooly, Youlia,Rozen, Shlomo

, p. 6780 - 6783 (2008/12/22)

(Chemical Equation Presented) A general preparation for aromatic and aliphatic, cyclic as well as linear, symmetric and asymmetric difluoromethylenedioxy derivatives is described. The alcohols were reacted with thiophosgene to give thiocarbonates, which in turn were reacted with BrF 3. The fluorination step is complete in seconds with moderate to high yields under mild conditions.

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