14366-66-6 Usage
Chemical structure
Benzene derivative with two chlorine atoms and a thioether group
Explanation
Different sources of media describe the Explanation of 14366-66-6 differently. You can refer to the following data:
1. The compound is derived from benzene, which is a six-carbon ring with alternating single and double bonds. It has two chlorine atoms and a thioether group (a sulfur atom bonded to two carbon atoms) attached to the benzene ring.
2. The compound contains two functional groups chloro (Cl) and thioether (S-alkyl). These groups give the compound its specific chemical properties and reactivity.
3. The compound is used as a starting material or intermediate in the production of various chemicals, including those used in the pharmaceutical, agricultural, and dye industries.
4. The presence of chloro and thioether groups in the compound makes it potentially hazardous. It should be handled with care to avoid exposure and minimize the risk of adverse health effects.
5. Due to its hazardous nature, it is essential to follow proper handling procedures, such as wearing protective gear and working in a well-ventilated area, to minimize the risk of exposure to the compound.
Functional groups
Chloro and thioether groups
Applications
Synthesis of pharmaceuticals, agricultural products, dyes, and organic compounds
Hazardous nature
Potential health risks due to chloro and thioether groups
Handling precautions
Careful handling to avoid exposure
Check Digit Verification of cas no
The CAS Registry Mumber 14366-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,6 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14366-66:
(7*1)+(6*4)+(5*3)+(4*6)+(3*6)+(2*6)+(1*6)=106
106 % 10 = 6
So 14366-66-6 is a valid CAS Registry Number.
14366-66-6Relevant articles and documents
Synthesis and QSAR studies on hypotensive 1-[3-(4-substituted phenylthio) propyl]-4-(substituted phenyl) piperazines
Saxena, Anil K.,Rao, Jyoti,Chakrabarty, Ruchika,Saxena, Mridula,Srimal
, p. 1708 - 1712 (2007)
A series of 1-[3-(4-substituted phenylthio) propyl]-4-(substituted phenyl) piperazines has been synthesized and evaluated for hypotensive activity. The QSAR studies indicate that resonance and hydrophobic parameters of the aryl substituents are important
Hexitol derivatives having vasodilative activity
-
, (2008/06/13)
Disclosed is a hexitol derivative represented by the formula (I): STR1 wherein Q represents a formula selected from the group consisting of STR2 wherein a represents NH, O or S; each of b, c and d independently represents CH or N; each of R1, R2, R3 and R4 independently represents hydrogen, lower alkyl, trifluoromethyl, aryl, lower alkanoyloxy, amino, lower alkylamino, lower alkanoylamino, lower alkanoyl, aroyl, halogen, nitro, (CH2)m OR 7, (CH2)m SR7, (CH2)m CO2 R7 where R7 represents hydrogen or lower alkyl and m represents an integer of 0 to 3; each of R5 and R6 independently represents hydrogen or lower alkyl; U represents >N-- or STR3 W represents a single bond, --O-- or --S--; X represents STR4 wherein each of Y1 and Y2 independently represents hydrogen, lower alkyl, hydroxyl, lower alkanoyloxy, nitrile or phenyl; or Y1 and Y2 are combined together to form oxygen; each of Y3 and Y4 independently represents hydrogen or lower alkyl; and l is an integer of 0 to 6, and where l is an integer of 2 to 6, each STR5 may be the same or different; Z represents hydrogen or nitro; and, n is 2 or 3 or a pharmaceutically acceptable salt thereof. The compounds show prominent coronary vasodilative activities, and are useful in treating angina pectoris and myocardial infarction.
