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4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is a chemical compound with the molecular formula C14H9F3NO2. It is a nitro-substituted biphenyl derivative known for its trifluoromethyl group, which significantly enhances its chemical reactivity. 4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is widely recognized as a valuable building block in organic synthesis for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Its utility as a pharmaceutical intermediate and its role in the development of new materials and technologies further underscore its importance in the chemical industry. However, due to potential hazards to human health and the environment, careful handling is advised.

346-99-6

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346-99-6 Usage

Uses

Used in Pharmaceutical Industry:
4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical properties allow for the creation of complex organic molecules that can address specific medical needs.
Used in Agrochemical Industry:
In the agrochemical sector, 4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features enable the production of effective compounds designed to protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is employed as a key intermediate in organic synthesis, facilitating the preparation of a wide range of fine chemicals. Its presence in these syntheses is crucial for achieving desired chemical structures and properties in the final products.
Used in Material Science:
4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl is also used in the development of new materials and technologies, where its unique structural attributes and reactivity can be leveraged to create innovative materials with specific properties for various applications.
Used as a Pharmaceutical Intermediate:
4'-Nitro-3-(trifluoroMethyl)-1,1'-biphenyl serves as an essential pharmaceutical intermediate, playing a critical role in the synthesis of active pharmaceutical ingredients. Its presence in these processes is vital for the production of effective medications and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 346-99-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 346-99:
(5*3)+(4*4)+(3*6)+(2*9)+(1*9)=76
76 % 10 = 6
So 346-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H8F3NO2/c14-13(15,16)11-3-1-2-10(8-11)9-4-6-12(7-5-9)17(18)19/h1-8H

346-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)-3-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 3'-trifluoromethyl-4-nitrobiphenyl

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:346-99-6 SDS

346-99-6Relevant academic research and scientific papers

Polyvinylpyridine, a versatile solid phase for coordinative immobilisation of palladium precatalysts - Applications in Suzuki-Miyaura reactions

Solodenko, Wladimir,Mennecke, Klaas,Vogt, Carla,Gruhl, Susan,Kirschning, Andreas

, p. 1873 - 1881 (2008/01/27)

The immobilisation of an oxime-based palladacycle on polyvinylpyridine (PVP) resin affords a reusable, air, moisture and thermally stable palladium precatalyst which exerts high activity in Suzuki-Miyaura reactions both in batch as well as continuous-flow processes. Evidence is presented which shows that, besides serving as an anchor for the precatalyst, PVP also acts as a scavenger for Pd particles present in solution. Georg Thieme Verlag Stuttgart.

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