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6008-75-9

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6008-75-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 13 hydrogen (H) atoms, 1 chlorine (Cl) atom, and 2 sulfur (S) atoms.
2. Heterocyclic Organic Compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements. In this case, the compound has a six-membered ring with two sulfur atoms, making it a heterocyclic organic compound.
3. Six-membered Ring

Explanation

The compound has a ring structure with six atoms, which is a common feature in many organic compounds.
4. Substituted with 4-chlorophenyl and phenyl groups

Explanation

The 1,3-dithiolane ring is substituted with two different aromatic groups a 4-chlorophenyl group (a phenyl group with a chlorine atom at the 4th position) and a phenyl group (a simple six-membered aromatic ring with alternating single and double carbon-carbon bonds).
5. Used in Organic Synthesis

Explanation

The compound serves as a building block or intermediate in the synthesis of more complex organic molecules.
6. Pharmaceutical Research

Explanation

It is used as a starting material or intermediate in the development of new pharmaceuticals, which can have various therapeutic applications.
7. Agrochemicals Preparation

Explanation

The compound is also used in the preparation of agrochemicals, which are chemicals used in agriculture to protect crops from pests, diseases, and other threats.
8. Potential Applications in Drug Development

Explanation

Due to its unique structure and properties, the compound has the potential to be used in the development of new drugs with novel therapeutic effects.
9. Biological and Pharmacological Properties

Explanation

The compound is studied for its interactions with biological systems and its potential effects on living organisms, which can be useful in understanding its therapeutic potential.
10. Reagent in Chemical Reactions

Explanation

The compound's unique structure and properties make it a valuable reagent in various chemical reactions, facilitating the synthesis of other compounds or aiding in the study of reaction mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 6008-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6008-75:
(6*6)+(5*0)+(4*0)+(3*8)+(2*7)+(1*5)=79
79 % 10 = 9
So 6008-75-9 is a valid CAS Registry Number.

6008-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-2-phenyl-1,3-dithiolane

1.2 Other means of identification

Product number -
Other names 1,3-Dithiolane,2-(4-chlorophenyl)-2-phenyl

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:6008-75-9 SDS

6008-75-9Relevant articles and documents

Catalysis by Solid Superacids; 8. Improved Nafion-H Perfluorinated Resinsulfonic Acid-Catalyzed Preparation of Dimethyl Acetals and Ethylenedithioacetals, and Hydrolysis of Dimethyl Acetals

Olah, George A.,Narang, Subhash C.,Meidar, David,Salem, George F.

, p. 282 - 283 (1981)

-

Silica-supported phosphorus pentoxide: A reusable catalyst for S,S-acetalization of carbonyl groups under ambient conditions

Shaterian, Hamid Reza,Azizi, Kobra,Fahimi, Nafiseh

experimental part, p. 85 - 91 (2012/01/06)

Phosphorus pentoxide supported on silica gel (P2O 5/SiO2) efficiently acts as a highly active and reusable catalyst for cyclic and non-cyclic S,S-acetalization of a variety of carbonyl compounds under mild, solvent-free an

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