96147-14-7 Usage
Structure
Cyclohexane ring with four chlorine atoms and two carbonyl groups
3. Derivative of cyclohexanedione
Explanation
1,2-Cyclohexanedione, 3,3,6,6-tetrachlorois derived from cyclohexanedione, which is a six-membered ring with two carbonyl groups.
Explanation
This compound is used as a reagent in various organic synthesis processes, which involve the formation of new chemical compounds from simpler ones.
5. Use in pharmaceuticals and agrochemicals production
Explanation
The compound has applications in the production of pharmaceuticals (drugs) and agrochemicals (chemicals used in agriculture, such as pesticides and fertilizers).
6. Environmental pollutant
Explanation
1,2-Cyclohexanedione, 3,3,6,6-tetrachlorois considered a potential environmental pollutant due to its toxic and hazardous properties.
7. Regulation by environmental protection agencies
Explanation
Due to its harmful effects on human health and the environment, this compound is regulated by environmental protection agencies to control its use and disposal.
8. Toxic and hazardous properties
Explanation
Studies have shown that 1,2-Cyclohexanedione, 3,3,6,6-tetrachlorocan have harmful effects on both human health and the environment, making it a toxic and hazardous substance.
9. Caution in handling and use
Explanation
Because of its toxic and hazardous properties, caution should be exercised when handling and using this compound to minimize the risk of exposure and environmental contamination.
Application
Reagent in organic synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 96147-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,4 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96147-14:
(7*9)+(6*6)+(5*1)+(4*4)+(3*7)+(2*1)+(1*4)=147
147 % 10 = 7
So 96147-14-7 is a valid CAS Registry Number.
96147-14-7Relevant articles and documents
PRACTICAL SYNTHESIS OF 2,2,5,5-TETRACHLORO-1,6-HEXANEDIOIC ACID, FROM TRANS-1,2-CYCLOHEXANEDIOL OR CYCLOHEXANONE, INVOLVING OXIDATION OF 3,3,6,6-TETRACHLORO-1,2-CYCLOHEXANEDIONE
Buyck, Laurent de,Vanslembrouck, Jan,Kimpe, Norbert de,Verhe, Roland,Schamp, Niceas
, p. 913 - 918 (2007/10/02)
Trans-1,2-cyclohexanediol was quantitatively converted into 3,3,6,6-tetrachloro-1,2-cyclohexanedione (2) by treatment with chlorine in dimethylformamide.The hydrate of the dione was oxidized by aqueous potassium permanganate to afford the title acid 1 in 91percent overall yield.An alternative low cost preparation was elaborated, providing 2 in 61-74percent yield starting from cyclohexanone in a three step procedure without isolation of intermediates.The reaction seqence involves substitution of α-dichloro- and trichlorocyclohexanones by sodium acetate in acetic acid and chlorination of the resulting 2-hydroxy- and 2-acetoxy-2-cyclohexenones in dimethylformamide.
