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315-14-0

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315-14-0 Usage

Description

1,3,5-Trifluoro-2-nitrobenzene is an organic compound with the chemical formula C6H3F3NO2. It is a clear yellow liquid and is known for its unique chemical properties, which make it a valuable intermediate in the synthesis of various compounds, particularly in the pharmaceutical and chemical industries.

Uses

Used in Pharmaceutical Industry:
1,3,5-Trifluoro-2-nitrobenzene is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential applications in treating a wide range of medical conditions.
Used in Chemical Industry:
1,3,5-Trifluoro-2-nitrobenzene is used as a building block in the synthesis of various chemical compounds, including agrochemicals, dyes, and other specialty chemicals. Its versatility in chemical reactions makes it a valuable asset in the development of new products with specific properties and applications.
Used in Research and Development:
1,3,5-Trifluoro-2-nitrobenzene is also utilized in research and development laboratories for the exploration of new chemical reactions and the synthesis of novel compounds. Its unique properties make it an attractive candidate for studying various aspects of organic chemistry, such as reaction mechanisms, stereochemistry, and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 315-14-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 315-14:
(5*3)+(4*1)+(3*5)+(2*1)+(1*4)=40
40 % 10 = 0
So 315-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H2F3NO2/c7-3-1-4(8)6(10(11)12)5(9)2-3/h1-2H

315-14-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A17035)  1,3,5-Trifluoro-2-nitrobenzene, 98%   

  • 315-14-0

  • 1g

  • 242.0CNY

  • Detail
  • Alfa Aesar

  • (A17035)  1,3,5-Trifluoro-2-nitrobenzene, 98%   

  • 315-14-0

  • 5g

  • 874.0CNY

  • Detail
  • Alfa Aesar

  • (A17035)  1,3,5-Trifluoro-2-nitrobenzene, 98%   

  • 315-14-0

  • 25g

  • 3519.0CNY

  • Detail
  • Aldrich

  • (261807)  2,4,6-Trifluoronitrobenzene  98%

  • 315-14-0

  • 261807-5G

  • 734.76CNY

  • Detail

315-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Trifluoro-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1,3,5-trifluoro-2-nitro-benzene

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:315-14-0 SDS

315-14-0Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

-

Paragraph 00846, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Chemistry of superacids: 35. * NO2Cl-3MXN systems: Superelectrophilic aprotic nitrating agents for deactivated aromatics

Olah,Orlinkov,Ramaiah,Oxyzoglou,Prakash

, p. 924 - 927 (2007/10/03)

Superelectrophilic nitration of deactivated aromatics with NO2Cl-3MXn complexes in aprotic nonpolar solvents such as CH2Cl2 makes it possible to obtain the corresponding nitro derivatives in good to almost quantitative yields under mild conditions.

The effect of fluorine substitution on the physicochemical properties and the analgesic activity of paracetamol

Barnard,Storr,O'Neill,Park

, p. 736 - 744 (2007/10/02)

The physicochemical properties and analgesic action of six fluorinated analogues of 4-hydroxyacetanilide (paracetamol) have been investigated. Fluorine substitution adjacent to the hydroxyl group increased lipophilicity and oxidation potential whilst substitution adjacent to the amide had little effect on lipophilicity but led to a greater increase in oxidation potential. Lack of coplanarity and conjugation of the amide group and aromatic ring was also apparent with the analogues that had fluorine in the 2 and 6 positions. Introduction of fluorine into the amide group of paracetamol increased the lipophilicity 4-fold and also increased the oxidation potential of paracetamol. ED50 values for analgesic activity in the phenylquinone-induced abdominal constriction test on male Swiss White mice showed that ring substitution by fluorine reduced activity, especially at the 2,6-positions. Introduction of fluorine into the amide group enhanced activity significantly. Correlation of the analgesic activity with the physicochemical properties indicated that conjugation (and planarity) of the amide group with the aromatic ring is essential for activity and that ease of oxidation may also be an important factor.

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