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364-13-6

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364-13-6 Usage

Chemical Properties

white to light yellow crystal powder

General Description

2-(Trifluoromethyl)-1,4-phenylenediamine (2,5-Diaminobenzotrifluoride, 2-(trifluoromethyl)benzene-1,4-diamine) can be prepared from 5-acetamido-2-aminobenzotrifluoride.

Check Digit Verification of cas no

The CAS Registry Mumber 364-13-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 364-13:
(5*3)+(4*6)+(3*4)+(2*1)+(1*3)=56
56 % 10 = 6
So 364-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F2NO3/c7-3-1-4(8)6(10)5(2-3)9(11)12/h1-2,10H

364-13-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L10009)  2-Trifluoromethyl-p-phenylenediamine, 99%   

  • 364-13-6

  • 1g

  • 909.0CNY

  • Detail
  • Alfa Aesar

  • (L10009)  2-Trifluoromethyl-p-phenylenediamine, 99%   

  • 364-13-6

  • 5g

  • 3241.0CNY

  • Detail
  • Aldrich

  • (540439)  2-(Trifluoromethyl)-1,4-phenylenediamine  97%

  • 364-13-6

  • 540439-1G

  • 823.68CNY

  • Detail

364-13-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Trifluoromethyl)Benzene-1,4-Diamine

1.2 Other means of identification

Product number -
Other names 2-(Trifluoromethyl)benzene-1,4-diamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:364-13-6 SDS

364-13-6Relevant articles and documents

A Mild, DNA-compatible nitro reduction using B2(OH)4

Du, Huang-Chi,Simmons, Nicholas,Faver, John C.,Yu, Zhifeng,Palaniappan, Murugesan,Riehle, Kevin,Matzuk, Martin M.

, p. 2194 - 2199 (2019)

A hypodiboric acid system for the reduction of nitro groups on DNA-chemical conjugates has been developed. This transformation provided good to excellent yields of the reduced amine product for a variety of functionalized aromatic, heterocyclic, and aliphatic nitro compounds. DNA tolerance to reaction conditions, extension to decigram scale reductions, successful use in a DNA-encoded chemical library synthesis, and subsequent target selection are also described.

Activated Mont K10-Carbon supported Fe2O3: A versatile catalyst for hydration of nitriles to amides and reduction of nitro compounds to amines in aqueous media

Rahman, Taskia,Borah, Geetika,Gogoi, Pradip K

, (2021/03/14)

The iron oxide was successfully supported on activated clay/carbon through an experimentally viable protocol for both hydrations of nitrile to amide and reduction of nitro compounds to amines. The as-prepared catalyst has been extensively characterised by XPS, SEM-EDX, TEM, TGA, BET surface area measurements and powdered X-ray diffraction (PXRD). A wide variety of substrates could be converted to the desired products with good to excellent yields by using water as a green solvent for both the reactions. The catalyst was recyclable and reusable up to six consecutive cycles without compromising its catalytic proficiency. Graphical abstract: Activated Mont K10 carbon-supported Fe2O3 is a very efficient and versatile heterogeneous catalytic system for hydration of nitriles to amides and reduction of nitro compounds to amines and can be reused up to six consecutive cycles without significant loss in catalytic activity.[Figure not available: see fulltext.].

Nanoscale Fe2O3-based catalysts for selective hydrogenation of nitroarenes to anilines

Jagadeesh, Rajenahally V.,Surkus, Annette-Enrica,Junge, Henrik,Pohl, Marga-Martina,Radnik, Joerg,Rabeah, Jabor,Huan, Heming,Schunemann, Volker,Brueckner, Angelika,Beller, Matthias

, p. 1073 - 1076 (2014/01/06)

Production of anilines - key intermediates for the fine chemical, agrochemical, and pharmaceutical industries - relies on precious metal catalysts that selectively hydrogenate aryl nitro groups in the presence of other easily reducible functionalities. Herein, we report convenient and stable iron oxide (Fe2O3) - based catalysts as a more earth-abundant alternative for this transformation. Pyrolysis of iron-phenanthroline complexes on carbon furnishes a unique structure in which the active Fe2O 3 particles are surrounded by a nitrogen-doped carbon layer. Highly selective hydrogenation of numerous structurally diverse nitroarenes (more than 80 examples) proceeded in good to excellent yield under industrially viable conditions.

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