Welcome to LookChem.com Sign In|Join Free
  • or
4-Amino-6-fluoro-2-methylquinoline, a quinoline derivative with the chemical formula C10H8FN2, features a fluorine atom at the 6 position and a methyl group at the 2 position. 4-AMINO-6-FLUORO-2-METHYLQUINOLINE is recognized for its unique structure and properties, positioning it as a promising candidate for research and development in medicinal chemistry.

288151-49-5

Post Buying Request

288151-49-5 Suppliers

Recommended suppliers

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

288151-49-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-6-fluoro-2-methylquinoline serves as a valuable intermediate for the synthesis of other organic compounds, playing a crucial role in the development of new drugs. Its distinctive chemical structure contributes to its potential applications in creating innovative pharmaceuticals.
Used in Medicinal Chemistry Research:
4-AMINO-6-FLUORO-2-METHYLQUINOLINE is utilized in the study and treatment of various diseases, such as malaria and cancer. The exploration of 4-amino-6-fluoro-2-methylquinoline's potential in medicinal chemistry is ongoing, with the aim of discovering its full therapeutic capabilities and enhancing its utility in healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 288151-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,1,5 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 288151-49:
(8*2)+(7*8)+(6*8)+(5*1)+(4*5)+(3*1)+(2*4)+(1*9)=165
165 % 10 = 5
So 288151-49-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9FN2/c1-6-4-9(12)8-5-7(11)2-3-10(8)13-6/h2-5H,1H3,(H2,12,13)

288151-49-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (BBO000077)  4-Amino-6-fluoro-2-methylquinoline  AldrichCPR

  • 288151-49-5

  • BBO000077-1G

  • 2,255.76CNY

  • Detail

288151-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-2-methylquinolin-4-amine

1.2 Other means of identification

Product number -
Other names QU190

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:288151-49-5 SDS

288151-49-5Downstream Products

288151-49-5Relevant academic research and scientific papers

Microwave-assisted synthesis of 4-quinolylhydrazines followed by nickel boride reduction: a convenient approach to 4-aminoquinolines and derivatives

Gemma, Sandra,Kukreja, Gagan,Tripaldi, Pierangela,Altarelli, Maria,Bernetti, Matteo,Franceschini, Silvia,Savini, Luisa,Campiani, Giuseppe,Fattorusso, Caterina,Butini, Stefania

, p. 2074 - 2077 (2008/09/18)

Nickel(II) chloride/sodium borohydride combination was employed for the reduction of 4-hydrazinoquinoline derivatives to the corresponding anilines. This reductive protocol was efficiently applied for the reductive cleavage of monosubstituted hydrazines. We described herein the microwave-assisted synthesis of 4-hydrazinoquinolines, which furnished a high yielding and rapid two-step procedure for the synthesis, under mild conditions, of 4-aminoquinolines as antimalarial precursors.

Phenyl urea and phenyl thiourea derivatives as orexin receptor antagonists

-

Page/Page column 17, (2010/02/05)

The present invention provides phenyl urea and phenyl thiourea derivatives which are non-peptide antagonists of human orexin receptors, in particular orexin-1 receptors, of formula (I) in which: Z represents oxygen or sulfur; and R1to R7represent various substituent groups; and pharmaceutically acceptable salts thereof. In particular, these compounds are of potential use in the treatment of obesity including obesity observed in Type 2(non-insulin-dependent) diabetes patients and/or sleep disorders.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 288151-49-5