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2,5-dinitro-3,6-diphenyl-1,4-dithiine is a complex organic compound characterized by its unique molecular structure. It features a 1,4-dithiin backbone, which consists of two sulfur atoms connected by a chain of four carbon atoms. The compound is further distinguished by the presence of two nitro groups (-NO2) at the 2nd and 5th positions, and two phenyl rings (C6H5) attached to the 3rd and 6th carbon atoms. This chemical structure endows the compound with specific properties, such as its potential reactivity and stability, which can be relevant in various chemical and industrial applications. The compound's formula is C16H10N2O4S2, reflecting its composition of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms.

7402-85-9

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7402-85-9 Usage

Organic compound

Consisting of carbon, hydrogen, and other elements 2,5-dinitro-3,6-diphenyl-1,4-dithiine is an organic compound as it is primarily made up of carbon and hydrogen atoms, along with other elements such as nitrogen, oxygen, and sulfur.

Two nitro groups

Nitro groups (-NO2) The compound contains two nitro groups, which are functional groups consisting of an oxygen-nitrogen-oxygen arrangement. These groups are known to impart explosive and unstable properties to certain compounds.

Two phenyl rings

Aromatic carbon rings (C6H5) The compound has two phenyl rings, which are six-carbon aromatic rings with delocalized electrons. Phenyl rings are common structural elements in many organic compounds and contribute to the compound's stability and chemical properties.

Dithiine ring

A ring structure containing sulfur atoms The 1,4-dithiine component of the compound is a five-membered ring containing two sulfur atoms. This ring structure contributes to the compound's unique chemical properties and potential applications.

Research and laboratory use

Building block for synthesis 2,5-dinitro-3,6-diphenyl-1,4-dithiine is primarily used in research and laboratory settings as a building block for the synthesis of more complex organic compounds, making it a valuable tool in organic chemistry.

Yellow crystalline appearance

Visual characteristic 2,5-dinitro-3,6-diphenyl-1,4-dithiine is known for its yellow crystalline appearance, which is a visual characteristic that can be helpful in identifying the compound.

Relatively high stability

Under normal conditions The compound exhibits relatively high stability under normal conditions, making it a suitable candidate for use in various research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7402-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7402-85:
(6*7)+(5*4)+(4*0)+(3*2)+(2*8)+(1*5)=89
89 % 10 = 9
So 7402-85-9 is a valid CAS Registry Number.

7402-85-9SDS

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 2,5-dinitro-3,6-diphenyl-1,4-dithiine

1.2 Other means of identification

Product number -
Other names 1,4-Dithiin,2,5-dinitro-3,6-diphenyl

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:7402-85-9 SDS

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