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3,3-Dichlorothietane-1,1-dioxide is a chemical compound characterized by its molecular formula C2H2Cl2O2. It presents as a colorless or pale yellow liquid with a distinct pungent odor. 3,3-Dichlorothietane-1,1-dioxide is recognized for its role as a chemical intermediate in various industrial applications, particularly in the production of pharmaceuticals and agricultural chemicals. Additionally, it finds use as a solvent and in the synthesis of other organic compounds. Due to its moderately toxic nature, it is essential to exercise caution during handling to prevent irritation to the skin, eyes, and respiratory tract, as well as to avoid ingestion, inhalation, or skin absorption.

90344-85-7

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90344-85-7 Usage

Uses

Used in Pharmaceutical Industry:
3,3-Dichlorothietane-1,1-dioxide is utilized as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to serve as a building block in the creation of new and existing medications, contributing to the development of novel treatments and therapies.
Used in Agricultural Chemical Industry:
In the agricultural sector, 3,3-Dichlorothietane-1,1-dioxide is employed as a chemical intermediate in the production of agricultural chemicals. Its properties make it suitable for the synthesis of compounds that can be used in pest control, crop protection, and other agricultural applications, thereby supporting sustainable farming practices.
Used as a Solvent:
3,3-Dichlorothietane-1,1-dioxide is also used as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a versatile component in the manufacturing of different products, from industrial chemicals to consumer goods.
Used in Synthesis of Other Organic Compounds:
3,3-Dichlorothietane-1,1-dioxide is further utilized in the synthesis of other organic compounds, showcasing its versatility in organic chemistry. Its reactivity and functional groups make it a valuable precursor in the preparation of a variety of organic molecules for diverse applications.
Safety Precautions:
Given the moderately toxic nature of 3,3-Dichlorothietane-1,1-dioxide, it is crucial to implement proper safety measures during its handling, storage, and use. This includes wearing appropriate personal protective equipment, such as gloves, goggles, and respirators, to minimize the risk of skin, eye, and respiratory irritation. Additionally, it is important to follow guidelines for safe handling, storage, and disposal to prevent accidental ingestion, inhalation, or skin absorption.

Check Digit Verification of cas no

The CAS Registry Mumber 90344-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90344-85:
(7*9)+(6*0)+(5*3)+(4*4)+(3*4)+(2*8)+(1*5)=127
127 % 10 = 7
So 90344-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H4Cl2O2S/c4-3(5)1-8(6,7)2-3/h1-2H2

90344-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dichlorothietane 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 3,3-dichloro-thietane 1,1-dioxide

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:90344-85-7 SDS

90344-85-7Downstream Products

90344-85-7Relevant academic research and scientific papers

Reactions of 3-Chloro-2H-thiete 1,1-Dioxide

Sedergran, Thomas C.,Yokoyama, Masataka,Dittmer, Donald C.

, p. 2408 - 2412 (2007/10/02)

3-Chloro-2H-thiete 1,1-dioxide, prepared by dichlorination of thietane 1,1-dioxide followed by dehydrochlorination, reacts with carbanions, amines, alcohols, and thiols to give 3-substituted thietane or 2H-thiete 1,1-dioxides.For example, reaction with the anion of dimethyl or diethyl malonate gives 3-thietane 1,1-dioxide. 3-Chloro-2H-thiete 1,1-dioxide also undergoes Diels-Ader reactions with butadiene and 1,3-diphenylisobenzofuran. 2,3-Dibromothietane 1,1-dioxide, 2,3-dibromo-3-chlorothietane 1,1-dioxide, 2-bromo-2H-thiete 1,1-dioxide, and 2-bromo-3-chloro-2H-thiete 1,1-dioxide also have been prepared.

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