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1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is a chemical compound with the molecular formula C8H8FNO2. It is a nitrobenzene derivative featuring a fluorine atom and two methyl groups attached to the benzene ring. Available in a high purity of 98%, 1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is well-suited for various chemical reactions and processes, including the synthesis of other organic compounds and as a reagent in chemical research and development. Its elevated purity level ensures reliable use in both laboratory settings and industrial applications.

315-13-9

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315-13-9 Usage

Uses

1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure with a fluorine atom and methyl groups provides versatility in chemical reactions, making it a valuable component in the creation of new molecules with specific properties.
Used in Chemical Research and Development:
1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% serves as a reagent in chemical research and development, facilitating the exploration of new chemical pathways and the discovery of novel compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is used as a building block for the development of new drugs. Its structural features can be leveraged to create molecules with specific biological activities, contributing to the advancement of medicinal chemistry.
Used in Material Science:
1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is utilized in material science for the development of new materials with tailored properties. Its incorporation into polymers or other materials can lead to the creation of substances with improved characteristics for specific applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% may be employed as a precursor in the synthesis of active ingredients for pesticides or other agricultural chemicals, contributing to the development of more effective and targeted products for crop protection.
Used in Dye and Pigment Industry:
1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98% is used in the dye and pigment industry for the production of colorants with specific properties. Its chemical structure can be modified to create dyes or pigments with unique color characteristics and stability for use in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 315-13-9 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 315-13:
(5*3)+(4*1)+(3*5)+(2*1)+(1*3)=39
39 % 10 = 9
So 315-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8FNO2/c1-5-3-6(2)8(10(11)12)7(9)4-5/h3-4H,1-2H3

315-13-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H27762)  1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98%   

  • 315-13-9

  • 1g

  • 910.0CNY

  • Detail
  • Alfa Aesar

  • (H27762)  1-Fluoro-3,5-dimethyl-2-nitrobenzene, 98%   

  • 315-13-9

  • 5g

  • 3365.0CNY

  • Detail

315-13-9SDS

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-fluoro-3,5-dimethyl-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-Fluor-3,5-dimethyl-2-nitro-benzol

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:315-13-9 SDS

315-13-9Relevant academic research and scientific papers

π-face donor properties of N-heterocyclic carbenes in grubbs II complexes

Leuthaeusser, Steffen,Schmidts, Volker,Thiele, Christina M.,Plento, Herbert

experimental part, p. 5465 - 5481 (2009/06/06)

The electron-donating properties of eighteen N-heterocyclic carbenes (N,N′-bis(2,6-dimethylphenyl)imidazol)-2-ylidene and the respective dihydro ligands) with 4,4′-R substituted aryl rings (4,4′-R = NEt2, OMe, Me, H, SMe, F, Cl, Br, I) in the r

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