5409-96-1 Usage
Explanation
Different sources of media describe the Explanation of 5409-96-1 differently. You can refer to the following data:
1. The compound is composed of 16 carbon atoms, 16 hydrogen atoms, 2 chlorine atoms, and 2 sulfur atoms.
2. The core structure of the compound is a benzene ring, which is a six-carbon ring with alternating single and double bonds. A chlorine atom is attached at the first position (1-chloro), and two sulfur-containing groups are connected to the benzene ring.
3. The compound is classified as a chlorinated aromatic compound because it has a chlorine atom (Cl) attached to the benzene ring.
4. The compound has two sulfur atoms (S) as part of its functional groups, which are connected to the benzene ring through carbon chains.
5. Due to its unique structure and properties, the compound can be used as a building block or intermediate in the synthesis of a wide range of organic compounds and materials. It may also have potential applications in the development of new drugs, agrochemicals, and other products in various industries.
6. The compound's structure is unique due to the presence of both chlorine and sulfur atoms, which can influence its reactivity, stability, and potential applications in different fields.
7. The material does not provide information about the compound's physical properties, such as melting point, boiling point, density, or solubility.
8. The material does not provide information about the compound's chemical properties, such as reactivity, stability, or potential reactions with other compounds.
9. The material does not provide information about the safety precautions or handling procedures for this compound. It is essential to follow proper safety protocols when working with chemicals, especially if they are toxic, corrosive, or reactive.
Molecular Structure
Benzene ring with a chlorine atom at position 1 and two sulfur-containing groups attached
Chlorinated Aromatic Compound
Contains a chlorine atom
Sulfur-Containing Functional Groups
Two sulfur atoms in the molecule
Potential Applications
Synthesis of various organic compounds and materials, pharmaceuticals, agrochemicals, and other industries
Unique Structure
Presence of chlorine and sulfur atoms in the molecule
Physical Properties
Not provided in the material
Chemical Properties
Not provided in the material
Safety and Handling
Not provided in the material
Check Digit Verification of cas no
The CAS Registry Mumber 5409-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5409-96:
(6*5)+(5*4)+(4*0)+(3*9)+(2*9)+(1*6)=101
101 % 10 = 1
So 5409-96-1 is a valid CAS Registry Number.
5409-96-1Relevant articles and documents
Ionic liquid as catalyst and reaction medium: A simple, convenient and green procedure for the synthesis of thioethers, thioesters and dithianes using an inexpensive ionic liquid, [pmIm]Br
Ranu, Brindaban C.,Jana, Ranjan
, p. 1811 - 1818 (2007/10/03)
An easily accessible and inexpensive room temperature ionic liquid, 1-pentyl-3-methylimidazolium bromide, [pmIm]Br efficiently catalyzes the reaction of alkyl halides or acyl halides with thiols without any solvent at room temperature leading to the synthesis of thioethers and thioesters in high yields. This reaction has also been extended for the preparation of dithianes and transthioetherification. The ionic liquid is recovered and recycled for subsequent runs.
1H- And13C-NMR and electron ionization (EI) mass spectrometric study of o- And p-substituted 1,n-diarylsulfonylalkanes, XC6H4so2(CH2)nso 2C6H4X (n = 2-5, 8, 10)+
Pihlaja, Kalevi,Kabilan, Senthamaraikannan,Ganapathi, Athiappan,Sankar, Punnaivanam
, p. 601 - 612 (2007/10/03)
1,n-Diphenylsulfonylalkanes, PhSO2(CH2)nSO2Ph (n =2-5, 8, 10) and their o- or p-Cl or -OMe derivatives were prepared and their 1H- and 13C-NMR and EI mass spectra recorded and analyzed. The chemical shifts of the aliphatic α- and β-carbons showed a clear dependence on the o-aryl substitution, the o-Cl being the most shielding for both. Clear low-field effects were found also for the aliphatic α-protons in o-Cl and o-OMe derivatives. In case of p-OMe derivatives a palpable shielding of the aliphatic α-protons was also found similarly to the β-protons of the o-OMe derivatives. Characteristic mass spectrometric fragmentations which reflected both the influence of the aryl substitution and the length of the alkyl chain were observed and sometimes also exhibited the sulphinic acid rearrangement.
Dipole Moments and UV Spectra of some Long-chain Molecules
Baliah, V.,Aparajithan, K.
, p. 255 - 259 (2007/10/02)
About one hundred compounds with long-chain molecular structure have been prepared (most of them are new).The dipole moments of four α,ω-bis(p-methoxyphenylthio)alkanes and five α,ω-bis(p-methoxyphenylsulphonyl)alkanes have been determined to find the effect of chain-length.In the case of sulphones, the observed values are compared with the values calculated for free rotation around all bonds intervening the end dipoles.The uv spectra of some 1,2-(distyrylsulphonyl)ethanes, and a number of α,ω-bis(arylsulphonyl)- and α,ω-bis(aryloxy)alkanes have been recorded to examine the applicability of the principle of chromophore additivity.
