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4-Fluoro-3-nitrotoluene, a chemical compound with the molecular formula C7H6FNO2, is a pale yellow solid. It is recognized for its role as an intermediate in the synthesis of various products, particularly in the pharmaceutical and agrochemical industries. Its chemical structure, incorporating both fluorine and nitro groups, lends it unique properties that are valuable in chemical reactions and product development.

446-11-7

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446-11-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Fluoro-3-nitrotoluene is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its presence in the molecular structure of these compounds can influence their pharmacological properties, such as potency, selectivity, and metabolic stability, making it a valuable component in drug development.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Fluoro-3-nitrotoluene serves as an essential intermediate in the production of pesticides and other agrochemicals. Its chemical properties allow for the creation of effective compounds designed to protect crops from pests and diseases, thereby contributing to increased agricultural productivity.
Used in Dye and Pigment Production:
4-Fluoro-3-nitrotoluene is also utilized as a starting material in the manufacture of dyes and pigments. Its unique combination of fluorine and nitro groups can impart specific color characteristics and stability to the final products, which is crucial for applications in textiles, plastics, and other industries that rely on colorants.
Safety and Handling:
Given its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system, 4-Fluoro-3-nitrotoluene is classified as a hazardous material. It is imperative to handle, store, and dispose of 4-Fluoro-3-nitrotoluene according to stringent safety protocols and regulations to minimize risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 446-11-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 446-11:
(5*4)+(4*4)+(3*6)+(2*1)+(1*1)=57
57 % 10 = 7
So 446-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6FNO2/c1-5-2-3-6(8)7(4-5)9(10)11/h2-4H,1H3

446-11-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H63317)  4-Fluoro-3-nitrotoluene, 98%   

  • 446-11-7

  • 25g

  • 600.0CNY

  • Detail
  • Alfa Aesar

  • (H63317)  4-Fluoro-3-nitrotoluene, 98%   

  • 446-11-7

  • 100g

  • 2401.0CNY

  • Detail

446-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-3-nitrotoluene

1.2 Other means of identification

Product number -
Other names 4-Fluoro-3-Nitrotoluene

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:446-11-7 SDS

446-11-7Relevant articles and documents

Selective small molecules blocking HIV-1 tat and coactivator PCAF association

Zeng, Lei,Li, Jiaming,Muller, Michaela,Yan, Sherry,Mujtaba, Shiraz,Pan, Chongfeng,Wang, Zhiyong,Zhou, Ming-Ming

, p. 2376 - 2377 (2007/10/03)

Development of drug resistance from mutations in the targeted viral proteins leads to continuation of viral production by chronically infected cells, contributing to HIV-mediated immune dysfunction. Targeting a host cell protein essential for viral reproduction, rather than a viral protein, may minimize the viral drug resistance problem as observed with HIV protease inhibitors. We report here the development of a novel class of N1-aryl-propane-1,3-diamine compounds using a structure-based approach that selectively inhibit the activity of the bromodomain of the human transcriptional co-activator PCAF, of which association with the HIV trans-activator Tat is essential for transcription and replication of the integrated HIV provirus. Copyright

Electrophilic nitration of aromatics in ionic liquid solvents

Laali,Gettwert

, p. 35 - 40 (2007/10/03)

Potential utility of a series of 1-ethyl-3-methylimidazolium salts [emim][X] with X = OTf-, CF3COO-, and NO3- as well as [HNEtPri2][CF3COO] (protonated Huenig's base) ionic liquids were explored as solvent for electrophilic nitration of aromatics using a variety of nitrating systems, namely NH4NO3/TFAA, isoamyl nitrate/BF3·Et2O, isoamyl nitrate/TfOH, Cu(NO3)/TFAA, and AgNO3/Tf2O. Among these, NH4NO3/TFAA (with [emim][CF3COO], [emim][NO3]) and isoamyl nitrate/BF3·Et2O, isoamyl nitrate/TfOH (with [emim][OTf]) provided the best overall systems both in terms of nitration efficiency and recycling/reuse of the ionic liquids. For [NO2][BF4] nitration, the commonly used ionic liquids [emim][AlCl4] and [emim][Al2Cl7] are unsuitable, as counterion exchange and arene nitration compete. [Emim][BF4] is ring nitrated with [NO2][BF4] producing [NO2-emim][BF4] salt, which is of limited utility due to its increased viscosity. Nitration in ionic liquids is surveyed using a host of aromatic substrates with varied reactivities. The preparative scope of the ionic liquids was also extended. Counterion dependency of the NMR spectra of the [emim][X] liquids can be used to gauge counterion exchange (metathesis) during nitration. Ionic liquid nitration is a useful alternative to classical nitration routes due to easier product isolation and recovery of the ionic liquid solvent, and because it avoids problems associated with neutralization of large quantities of strong acid.

2,3,4,4A-Tetrahydro-1H-pyrazino[1,2-a,]quinoxalin-5(6H)-ones and derivatives thereof for relieving hypertension

-

, (2008/06/13)

Compounds of the formula STR1 wherein R is hydrogen (lower)alkyl, phen(lower)alkyl, benzoyl(lower)alkyl, or p-halobenzoyl(lower)alkyl; R1 is hydrogen or (lower)alkyl; R2 is hydrogen, (lower)alkyl, (lower)alkoxy, chlorine, fluorine, trifluoromethyl, or amino in the 7-, 8-, or 9-position; R3 is hydrogen, or (lower)alkyl; and R4 is hydrogen, (lower)alkyl, (lower)alkoxy, chlorine, fluorine, or trifluoromethyl in the 7-, 8-, or 9-position; or the non-toxic acid addition salts thereof; exert a hypotensive effect in hypertensive animals.

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