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  • 717878-06-3 Structure
  • Basic information

    1. Product Name: 1-(4-fluorophenyl)-4-nitro-1H-iMidazole
    2. Synonyms: 1-(4-fluorophenyl)-4-nitro-1H-iMidazole
    3. CAS NO:717878-06-3
    4. Molecular Formula: C9H6FN3O2
    5. Molecular Weight: 207.1612432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 717878-06-3.mol
    9. Article Data: 4
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 366.7±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.43±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -1.29±0.61(Predicted)
    10. CAS DataBase Reference: 1-(4-fluorophenyl)-4-nitro-1H-iMidazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(4-fluorophenyl)-4-nitro-1H-iMidazole(717878-06-3)
    12. EPA Substance Registry System: 1-(4-fluorophenyl)-4-nitro-1H-iMidazole(717878-06-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 717878-06-3(Hazardous Substances Data)

717878-06-3 Usage

Description

1-(4-fluorophenyl)-4-nitro-1H-imidazole is a chemical compound with the molecular formula C9H6FN3O2, belonging to the nitroimidazole class. It features a nitro group and a fluorophenyl group, both of which contribute to its potential biological activity in medicinal chemistry. 1-(4-fluorophenyl)-4-nitro-1H-imidazole is recognized for its antimicrobial and antiprotozoal properties, making it a promising candidate for the development of new drugs to combat microbial infections and parasitic diseases.

Uses

Used in Pharmaceutical Industry:
1-(4-fluorophenyl)-4-nitro-1H-imidazole is used as a chemical intermediate for the development of new drugs due to its antimicrobial and antiprotozoal properties. Its potential application lies in creating medications to treat a variety of microbial infections and parasitic diseases, addressing the need for novel therapeutic options in this area.
Used in Medicinal Chemistry Research:
As a nitroimidazole derivative, 1-(4-fluorophenyl)-4-nitro-1H-imidazole serves as a subject of interest in medicinal chemistry research. Scientists are likely to explore its pharmacological properties, including how it interacts with biological targets and its potential therapeutic uses, to better understand its full range of applications in drug development.
Further research is necessary to fully comprehend the compound's pharmacological properties and its potential therapeutic uses, which could lead to significant advancements in the treatment of various diseases caused by microbial and parasitic pathogens.

Check Digit Verification of cas no

The CAS Registry Mumber 717878-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,7,8,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 717878-06:
(8*7)+(7*1)+(6*7)+(5*8)+(4*7)+(3*8)+(2*0)+(1*6)=203
203 % 10 = 3
So 717878-06-3 is a valid CAS Registry Number.

717878-06-3SDS

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 1-(4-fluorophenyl)-4-nitroimidazole

1.2 Other means of identification

Product number -
Other names 1-(4-fluorophenyl)-4-nitro-1H-imidazole

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:717878-06-3 SDS

717878-06-3Downstream Products

717878-06-3Relevant articles and documents

NOVEL COMPOUNDS

-

Page/Page column 133-134, (2016/04/20)

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase L1 (UCHL1). The invention further relates to the use of DUB inhibitors in the treatment of cancer and other indications. Compounds of the invention include compounds having the formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 to R8 are as defined herein.

Novel orally active NPY Y5 receptor antagonists: Synthesis and structure-activity relationship of spiroindoline class compounds

Sakamoto, Toshihiro,Moriya, Minoru,Tsuge, Hiroyasu,Takahashi, Toshiyuki,Haga, Yuji,Nonoshita, Katsumasa,Okamoto, Osamu,Takahashi, Hirobumi,Sakuraba, Aya,Hirohashi, Tomoko,Shibata, Takunobu,Kanno, Tetsuya,Ito, Junko,Iwaasa, Hisashi,Gomori, Akira,Ishihara, Akane,Fukuroda, Takahiro,Kanatani, Akio,Fukami, Takehiro

experimental part, p. 5015 - 5026 (2009/12/04)

Spiroindoline urea derivatives, designed to act as NPY Y5 receptor antagonists, were synthesized and their structure-activity relationships were investigated. Of these derivatives, compound 3a showed good Y5 binding affinity with favorable pharmacokinetic

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