Welcome to LookChem.com Sign In|Join Free

CAS

  • or

347-82-0

Post Buying Request

347-82-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

347-82-0 Usage

Description

Phenol, 4-fluoro-, 4-nitrobenzoate is a chemical compound that features a phenol core with a fluorine atom and a nitro group attached to a benzene ring. This molecule is known for its diverse applications in the fields of chemistry and medicine due to its unique combination of functional groups.

Uses

Used in Organic Synthesis:
Phenol, 4-fluoro-, 4-nitrobenzoate is utilized as a key intermediate in the synthesis of various organic compounds. Its presence in the molecule allows for a range of chemical reactions, making it a valuable building block in the creation of new molecules.
Used in Pharmaceutical Production:
Phenol, 4-fluoro-, 4-nitrobenzoate is employed as a precursor in the development of pharmaceuticals. Its unique structure contributes to the design of new drugs, particularly those targeting diseases such as cancer and inflammation. Phenol, 4-fluoro-, 4-nitrobenzoate's versatility in chemical reactions enables the creation of potential therapeutic agents.
Used in Dye Production:
In the dye industry, Phenol, 4-fluoro-, 4-nitrobenzoate is used as a starting material for the synthesis of various dyes. The presence of the phenol, fluorine, and nitro groups in the molecule allows for the creation of dyes with specific color properties and stability.
Used in Agrochemical Production:
Phenol, 4-fluoro-, 4-nitrobenzoate is also used in the agrochemical industry, where it serves as a building block for the development of new agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in crop protection and other agricultural applications.
Used in Cancer Treatment Research:
Phenol, 4-fluoro-, 4-nitrobenzoate has been studied for its potential use in the treatment of cancer. Its biological activities suggest that it may have therapeutic potential, and ongoing research is focused on understanding its mechanisms of action and potential applications in cancer therapy.
Used in Inflammation Treatment Research:
Similar to its potential use in cancer treatment, Phenol, 4-fluoro-, 4-nitrobenzoate is also being investigated for its potential role in the treatment of inflammation. Its unique structure and functional groups may contribute to anti-inflammatory effects, making it a subject of interest for researchers in the field of medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 347-82-0 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 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 347-82:
(5*3)+(4*4)+(3*7)+(2*8)+(1*2)=70
70 % 10 = 0
So 347-82-0 is a valid CAS Registry Number.

347-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-benzoic acid-(4-fluoro-phenyl ester)

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzoesaeure-(4-fluor-phenylester)

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:347-82-0 SDS

347-82-0Relevant articles and documents

Decarboxylative Hydroxylation of Benzoic Acids

Ritter, Tobias,Su, Wanqi,Xu, Peng

supporting information, p. 24012 - 24017 (2021/10/06)

Herein, we report the first decarboxylative hydroxylation to synthesize phenols from benzoic acids at 35 °C via photoinduced ligand-to-metal charge transfer (LMCT)-enabled radical decarboxylative carbometalation. The aromatic decarboxylative hydroxylation is synthetically promising due to its mild conditions, broad substrate scope, and late-stage applications.

Studies in organic fluorine compounds. Synthesis of fluorinated hydrazones, aryl esters of p halogenated phenols, fluorinated hydroxy ketones and their thiosemicarbazones and fluoro substituted thiazoles and their derivatives as possible fungicides

Srivastava,Bahel

, p. 841 - 845 (2007/10/10)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 347-82-0