34328-46-6 Usage
Uses
Used in Organic Synthesis:
4-Chloro-3-(trifluoromethyl)benzaldehyde is used as a key intermediate for the synthesis of various organic compounds. Its unique chemical structure allows for a wide range of reactions, making it a valuable building block in the creation of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-3-(trifluoromethyl)benzaldehyde is utilized as a crucial raw material for the development of new drugs. Its chemical properties enable it to be incorporated into the structures of various medicinal compounds, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemicals:
4-Chloro-3-(trifluoromethyl)benzaldehyde is also employed in the agrochemical sector as a starting material for the synthesis of various pesticides and other agricultural chemicals. Its reactivity and stability contribute to the development of effective products for crop protection and management.
Used in Dyestuff Industry:
In the dyestuff industry, 4-Chloro-3-(trifluoromethyl)benzaldehyde is used as an intermediate for the production of various dyes and pigments. Its distinct chemical structure allows for the creation of a wide array of colorants, enhancing the range of hues available for various applications, including textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 34328-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,2 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34328-46:
(7*3)+(6*4)+(5*3)+(4*2)+(3*8)+(2*4)+(1*6)=106
106 % 10 = 6
So 34328-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H4ClF3O/c9-7-2-1-5(4-13)3-6(7)8(10,11)12/h1-4H
34328-46-6Relevant articles and documents
Process for producing trifluoromethylbenzylamines
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, (2008/06/13)
The present invention relates to a process for producing a trifluoromethylbenzylamine represented by the general formula (1). This process includes the step of reducing an oxime represented by the general formula (2), where R1represents hydrogen atom, a halogen atom selected from the group consisting of fluorine, chlorine, bromine and iodine, or trifluoromethyl group, where R1is defined as above, and R2represents hydrogen atom, an alkyl group or an aralkyl group. With this process, the trifluoromethylbenzylamine can be produced with high selectivity.
Synthesis and Antimalarial Properties of 1-Imino Derivatives of 7-Chloro-3-substituted-3,4-dihydro-1,9(2H,10H)-acridinediones and Related Structures
Kesten, Stephen J.,Degnan, Margaret J.,Hung, Jocelyn,McNamara, Dennis J.,Ortwine, Daniel F.,et al.
, p. 3429 - 3447 (2007/10/02)
To improve upon the activity and properties of the 3-aryl-7-chloro-3,4-dihydro-1,9(2H,10H)-acridinediones, a variety of 1-imino derivatives (3) were prepared and shown to be highly active antimalarial agents in both rodents and primates.Among structural modifications prepared, including N10-alkyl and C2-substituted analogs, removal of the C9 oxygen, and introduction of an imino side chain at C9, the imines of the N10-H acridinediones were the most active compounds obtained.The imino derivative of7-chloro-3-(2,4-dichlorophenyl)-3,4-dihydro-1,9(2H,10H)-acridinedione (9aa) proved to be highly active in advanced studies in primates.
