34207-44-8

Usage

Uses

Used in Pharmaceutical and Agrochemical Production:
4-Chloro-3,5-diaminobenzotrifluoride is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Dye, Pigment, and Polymer Synthesis:
4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE is used as a building block in the production of dyes, pigments, and polymers, enhancing the color and properties of these materials.
Used in Fire Retardant Material Production:
4-Chloro-3,5-diaminobenzotrifluoride is used in the manufacturing of fire retardant materials, improving the safety and performance of various products.
Used as a Curing Agent in Epoxy and Urethane Resin Formulation:
4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE serves as a curing agent in the formulation of epoxies and urethane resins, enhancing the curing process and improving the final product's properties.
Used in High-Performance Coating and Adhesive Manufacturing:
4-Chloro-3,5-diaminobenzotrifluoride is used in the production of high-performance coatings and adhesives, providing improved adhesion, durability, and resistance to various environmental factors.

InChI:InChI=1/C7H6ClF3N2/c8-6-4(12)1-3(2-5(6)13)7(9,10)11/h1-2H,12-13H2

Upstream product

• 393-75-9 4-chloro-3,5-dinitrobenzotrifluoride 

Downstream Products

• 49635-57-6 (E)-2-[3-((E)-1,2-Bis-methoxycarbonyl-vinylamino)-2-chloro-5-trifluoromethyl-phenylamino]-but-2-enedioic acid dimethyl ester 
• 53882-21-6 diethyl N,N'-[2-chloro-5-(trifluoromethyl)-m-phenylene] dioxamate 
• 213269-79-5 Acetic acid [3-(2-acetoxy-acetylamino)-2-chloro-5-trifluoromethyl-phenylcarbamoyl]-methyl ester 
• 53882-20-5 N,N'-[2-chloro-5-(trifluoromethyl)-m-phenylene]dioxamic acid 
• 50594-82-6 1-trifluoromethyl-3,4,5-trichlorobenzene 

Relevant academic research and scientific papers

Double-Schiff base aluminum ion fluorescent probe Synthesis method and application thereof

The invention discloses a bis-Schiff base aluminum ion fluorescent probe as well as a synthesis method and application thereof, and belongs to the technical field of fluorescent probes. The chemical formula of the bis-Schiff base aluminum ion fluorescent

Preparation of 3,5-diaminobenzotrifluoride

3,5-Diaminobenzotrifluoride can be produced, in a single step, by reacting 4-chloro-3,5-dinitrobenzotrifluoride, in methanol, with hydrogen gas, in the presence of magnesium oxide, and in the presence of a catalyst comprising palladium on a carbon support.

Preparation of fluorine-containing diphenyl ethers

A method of preparing a diphenyl ether compound of the formula (II) STR1 wherein X is F, Cl or Br; Z is hydrogen, halogen, NO2 of CN; and W is methyl, cyano, CH3 CO--, or a group --C--OR, wherein R is --OH; --OM wherein M is a cation; OR1 wherein R1 is an optionally substituted aliphatic radical; --NR2 R3 wherein R2 and R3 are each hydrogen or an optionally substituted aliphatic radical; or --NHSO2 R4 wherein R4 is alkyl of 1 to 6 carbon atoms, which comprises reacting a 3-X-substituted-4,5-difluorobenzotrifluoride with a salt of a 3,4-W,Z-substituted phenol. The invention further comprises novel 3-X-4,5-difluorobenzotrifluorides for use in the process.

Cyano phenylene dioxamic molecules

Compounds represented below SPC1 And pharmaceutical compositions thereof, the compositions including the non-substituted phenylene dioxamates are useful in the prophylactic treatment of sensitized mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.

Derivatives of 4,6 dioxopyrido[3,2-g]quinoline 2,8 dicarboxylic acid

Novel chemical compounds of the formula: SPC1 Wherein R is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, phenyl, alkali metal, or an amine cation; X and Y can be the same or different and are selected from the group consisting of hydrogen, alkyl of from one to six carbon atoms, inclusive, cycloalkyl of 5 or 6 carbon atoms, inclusive, phenyl, hydroxyl, alkoxy having from one to three carbon atoms, inclusive, halogen, trifluoromethyl, cyano, carboxyamide and O C-OQ, EQU1 where Q is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, alkali metal, and an amine cation, with the proviso that where R is hydrogen, alkali metal or an amine cation, then Q is the same as R, and where R is phenyl or alkyl from one to three carbon atoms, then Q is phenyl or alkyl from one to three carbon atoms; and Z is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, and phenyl. The compounds are formulated with pharmaceutical carriers for oral or parenteral administration, with insufflation being the preferred method. The compositions are useful in the prophylactic treatment of sensitized humans and mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.