34207-44-8

Basic information

• Product Name: 4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE
• Synonyms: 2-CHLORO-4-TRIFLUOROMETHYL-1,3-PHENYLENEDIAMINE;2-CHLORO-1,3-DIAMINE-5-TRIFLUOROMETHYLBENZENE;2-CHLORO-5-TRIFLUOROMETHYL-BENZENE-1,3-DIAMINE;4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE;2-CHLORO-5-TRIFLUOROMETHYL-1,3-PHENYLENEDIAMINE;3,5-Diamino-4-Chorobenzotrifluoride;4-CHLORO-3,5-DIAMINOBENZOTRIFLUOROIDE
• CAS NO: 34207-44-8
• Molecular Formula: C₇H₆ClF₃N₂
• Molecular Weight: 210.58
• Mol File: 34207-44-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 91°C
• Boiling Point: 270.045 °C at 760 mmHg
• Flash Point: 117.12 °C
• Appearance: /
• Density: 1.51 g/cm³
• Vapor Pressure: 0.007mmHg at 25°C
• Refractive Index: 1.553
• PKA: 1.72±0.10(Predicted)
• CAS DataBase Reference: 4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE(34207-44-8)
• EPA Substance Registry System: 4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE(34207-44-8)

Safety Data

• Statements: 20/21/22-33-37
• Safety Statements: 22-36/37/39
• Hazardous Substances Data: 34207-44-8(Hazardous Substances Data)

Usage

General Description

4-Chloro-3,5-diaminobenzotrifluoride, also known as 4,4'-Diaminodiphenyl sulfone, is a chemical compound with the molecular formula C12H9ClF3N3. It is a white crystalline powder that is used as an intermediate in the production of various pharmaceuticals and agrochemicals. 4-CHLORO-3,5-DIAMINOBENZOTRIFLUORIDE is commonly utilized in the synthesis of dyes, pigments, and polymers. It is also a building block in the production of fire retardant materials and can be used as a curing agent in the formulation of epoxies and urethane resins. Additionally, it has applications in the manufacturing of high-performance coatings and adhesives. Overall, 4-Chloro-3,5-diaminobenzotrifluoride plays a crucial role in various industrial and chemical processes, making it a key compound in the field of chemistry and materials science.

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 articles and documents

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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.

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