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1,4-Dithiane, 2,3-dichloro-, trans- is a chemical compound with the molecular formula C4H8Cl2S2. It is a cyclic sulfur-containing compound, specifically a dithiane derivative, where two sulfur atoms are bonded to two carbon atoms, forming a four-membered ring. The trans-isomer indicates that the two chlorine atoms are positioned on opposite sides of the ring. 1,4-Dithiane, 2,3-dichloro-, trans- is known for its potential applications in organic synthesis and as a reagent in chemical reactions. It is important to handle this substance with care due to its potential toxicity and reactivity.

2040-67-7

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2040-67-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,4-Dithiane, 2,3-dichloro-, transhas 4 carbon atoms, 6 hydrogen atoms, 2 chlorine atoms, and 1 sulfur atom.

Explanation

This classification indicates that the compound contains a chlorine atom attached to an alkyl group (a carbon chain) and a sulfur atom, which is part of an ether functional group.

Explanation

The compound is in a liquid state at room temperature and appears clear and colorless, which means it does not have any visible color.

Explanation

The compound does not dissolve in water but can dissolve in organic solvents, such as alcohols, ethers, and hydrocarbons. This property is important for its use in chemical reactions and synthesis processes.

Explanation

1,4-Dithiane, 2,3-dichloro-, transis used as a starting material or building block in the production of various pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries.

Explanation

The compound is known for its reactivity, which allows it to participate in a range of chemical reactions. This includes the formation of carbon-carbon and carbon-sulfur bonds, making it a versatile molecule for creating complex organic compounds.

Classification

Chloroalkylthioether

Physical State

Clear, colorless liquid

Solubility

Insoluble in water, soluble in organic solvents

Applications

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Reactivity

Ability to undergo various reactions

Check Digit Verification of cas no

The CAS Registry Mumber 2040-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2040-67:
(6*2)+(5*0)+(4*4)+(3*0)+(2*6)+(1*7)=47
47 % 10 = 7
So 2040-67-7 is a valid CAS Registry Number.

2040-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2,3-Dichlor-1,4-dithian

1.2 Other means of identification

Product number -
Other names trans-2,3-dichloro-1,4-dithiane

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:2040-67-7 SDS

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