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(4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE is a chemical compound characterized by the presence of a fluorine and nitro group attached to a phenyl ring, along with a hydrazine functional group. (4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE is recognized for its reactivity and potential in the synthesis of biologically active molecules, making it a significant component in the fields of medicinal and agricultural chemistry.

289913-99-1

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289913-99-1 Usage

Uses

Used in Pharmaceutical Industry:
(4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE is used as a reagent for the synthesis of various pharmaceuticals. Its unique structure and reactive hydrazine group contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE is utilized as a reagent in the preparation of different agrochemicals. Its incorporation aids in the creation of compounds that can be used for pest control, crop protection, and other agricultural purposes.
Used in Research and Development:
(4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE serves as a valuable tool in the research and development of new compounds. Its structure and properties make it an essential component in studies of organic reactions and chemical transformations, furthering scientific understanding and innovation in chemistry.
Used in Organic Synthesis:
(4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE is also used as a building block in organic synthesis, where it plays a crucial role in the formation of various biologically active molecules. Its versatility and reactivity make it a sought-after component in the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 289913-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,9,1 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 289913-99:
(8*2)+(7*8)+(6*9)+(5*9)+(4*1)+(3*3)+(2*9)+(1*9)=211
211 % 10 = 1
So 289913-99-1 is a valid CAS Registry Number.

289913-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Fluoro-3-nitrophenyl)hydrazine

1.2 Other means of identification

Product number -
Other names (4-FLUORO-3-NITRO-PHENYL)-HYDRAZINE

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:289913-99-1 SDS

289913-99-1Upstream product

289913-99-1Relevant academic research and scientific papers

Inhibition of HIV-1 capsid assembly: Optimization of the antiviral potency by site selective modifications at N1, C2 and C16 of a 5-(5-furan-2-yl-pyrazol- 1-yl)-1H-benzimidazole scaffold

Tremblay, Martin,Bonneau, Pierre,Bousquet, Yves,Deroy, Patrick,Duan, Jianmin,Duplessis, Martin,Gagnon, Alexandre,Garneau, Michel,Goudreau, Nathalie,Guse, Ingrid,Hucke, Oliver,Kawai, Stephen H.,Lemke, Christopher T.,Mason, Stephen W.,Simoneau, Bruno,Surprenant, Simon,Titolo, Steve,Yoakim, Christiane

, p. 7512 - 7517 (2013/02/23)

A uHTS campaign led to the discovery of a 5-(5-furan-2-ylpyrazol-1-yl)-1H- benzimidazole series that inhibits assembly of HIV-1 capsid. Synthetic manipulations at N1, C2 and C16 positions improved the antiviral potency by a. The X-ray structure of 33 complexed with the capsid N-terminal domain allowed identification of major interactions between the inhibitor and the protein.

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