401-94-5

Basic information

• Product Name: 3-AMINO-5-NITROBENZOTRIFLUORIDE
• Synonyms: 3-AMINO-5-NITROBENZOTRIFLUORIDE;3-NITRO-5-(TRIFLUOROMETHYL)ANILINE;3-NITRO-5-TRIFLUOROMETHYL-PHENYLAMINE;3-Amino-5-Nitrobenzotrifluoride96%;3-Amino-5-nitrobenzotrifluoroide;3-Nitro-5-(trifluoromethyl)benzenamine;5-Nitro-α,α,α-trifluoro-m-toluidine;3-Amino-5-(Trifluoromethyl)nitrobenzene
• CAS NO: 401-94-5
• Molecular Formula: C₇H₅F₃N₂O₂
• Molecular Weight: 206.12
• Product Categories: Amines and Anilines;Fluorine series
• Mol File: 401-94-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 77-81°C
• Boiling Point: 280.7 °C at 760 mmHg
• Flash Point: 123.5 °C
• Appearance: /
• Density: 1.504 g/cm³
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 3-AMINO-5-NITROBENZOTRIFLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-5-NITROBENZOTRIFLUORIDE(401-94-5)
• EPA Substance Registry System: 3-AMINO-5-NITROBENZOTRIFLUORIDE(401-94-5)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39-36
• RIDADR: 2811
• HazardClass: 6.1
• PackingGroup: Ⅲ
• Hazardous Substances Data: 401-94-5(Hazardous Substances Data)

Usage

General Description

3-Amino-5-Nitrobenzotrifluoride is a specialized chemical compound. The molecular formula of this chemical is C7H5F3N2O2. It is commonly used in the manufacture or synthesis of various types of drugs and organic chemicals. It is also an essential compound in the pharmaceutical industry due to its properties and the reactions it creates. While the chemical may have numerous advantages due to its usage, it is also crucial to handle it responsibly due to its potentially hazardous nature. As with most chemical substances, appropriate safety measures are necessary while handling 3-Amino-5-Nitrobenzotrifluoride to prevent potential health risks. Specifics about its physical and chemical properties, stability, and reactivity need to be identified before use.

Upstream product

• 98-46-4 3-trifluoromethylnitrobenzene 
• 64-17-5 ethanol 
• 401-99-0 3,5-dinitrobenzotrifluoride 

Downstream Products

• 349-57-5 3-nitro-5-(trifluoromethyl)phenol 
• 401-93-4 5-chloro-3-trifluoromethyl-nitrobenzene 
• 402-00-6 acetic acid-(3-nitro-5-trifluoromethyl-anilide) 
• 2559-68-4 (3-nitro-5-trifluoromethyl-phenyl)-phenyl sulfone 
• 55225-67-7 3,3'-bis(trifluoromethyl)-5'-nitrocarbanilide 
• 618446-45-0 N-[3-nitro-5-(trifluoromethyl)phenyl]methanesulfonamide 
• 1044272-27-6 8-isopropyl-5-methyl-2-(3-nitro-5-trifluoromethyl-phenylamino)-7,8-dihydro-5H-pteridin-6-one 
• 1346448-26-7 2-((5-chloro-2-((3-nitro-5-(trifluoromethyl)phenyl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide 
• 795307-83-4 (3-amino-5-trifluoromethyl-phenyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

A Convenient, Efficient, and Environmentally Benign Method for Preparing Nitroanilines

An efficient method for the catalytic monoreduction of aromatic dinitro compounds to nitroanilines is reported. In the presence of selenium catalyst, the dinitroaromatic compounds are selectively reduced by CO/H2O to the corresponding nitroanilines under atmospheric pressure. The mono-reduction occurs in high selectivity regardless of the substitution groups on the aromatic ring without affecting other reducible functional groups.

Herbicidally active phenylsubstituted 5-and 6-membered heterocyclic compounds

A compound of formula (I): STR1 where E is oxygen or sulphur; A is CR3 or N where R3 is hydrogen or hydrocarbyl; D completes a 5 or 6-membered non-aromatic heterocyclic ring which optionally contains additional heteroatoms selected from oxygen, nitrogen or sulphur and which is optionally substituted by an optionally substituted lower hydrocarbyl group, or an optionally substituted heteroaryl group; R1 and R2 are each independently hydrogen; optionally substituted lower hydrocarbyl, or optionally substituted heteroaryl, or R1 and R2 together with the nitrogen atom to which they are attached, form a heterocyclic ring; Z represents halogen optionally substituted lower hydrocarbyl, optionally substituted lower hydocarbyloxy, optionally substituted lower hydrocarbylthio, hydrocarbylsulphinyl or hydrocarbylsulphonyl, cyano, nitro, CHO, NHOH, ONR7' R7", SF5 ; CO (optionally substituted lower hydrocarbyl), acylamino, COOR7, SO2 NR8 R9, CONR10 R11, OR12 or NR13 R14 where R7, R7', R7", R8, R9, R10 and R11 are independently hydrogen or lower hydrocarbyl; R12 is hydrogen; SO2 lower hydrocarbyl or COR15 ; R13 and R14 are independently lower hydrocarbyl, lower hydrocarbyloxy or a group R12 ; R15 is OR16, NR17 R18, hydrogen or lower hydrocarbyl; R16 is lower hydrocarbyl; R17 and R18 are independently hydrogen or lower hydrocarbyl; provided that when there are two or more substituents Z, they may be the same or different; and m is 0 or an integer from 1 to 5.