4-CHLORO-2-PHENYLQU...

4-CHLORO-2-PHENYLQUINAZOLINE

4-CHLORO-2-PHENYLQUINAZOLINE

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

4-CHLORO-2-PHENYLQUINAZOLINE 6484-25-9 4-CHLORO-2-PHENYLQUINAZOLINE

Quick Details

  • Appearance:slightly yellow to yellow crystalline powder
  • Application:For Organic Synthesis use
  • PackAge:IN 25kg drums
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation:As Per MSDS

Superiority:

4-CHLORO-2-PHENYLQUINAZOLINE Basic information
Product Name: 4-CHLORO-2-PHENYLQUINAZOLINE
Synonyms: AKOS 93518;AM-EX-OL(R);4-CHLORO-2-PHENYLQUINAZOLINE;QUINAZOLINE, 4-CHLORO-2-PHENYL-;4-CHLORO-2-PHENYLQUINAZOLINE OR AM-ex-OL;AM-EX-OL, 97% (4-CHLORO-2-PHENYL-QUINAZO LINE);am-ex-ol tm;4-CHLORO-2-PHENYLQUINAZOLINE 97%
CAS: 6484-25-9
MF: C14H9ClN2
MW: 240.69
EINECS: 229-346-2
Product Categories: Building Blocks;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Quinazolines;quinazoline
Mol File: 6484-25-9.mol
4-CHLORO-2-PHENYLQUINAZOLINE Structure

 

Details:

 
 
4-CHLORO-2-PHENYLQUINAZOLINE Chemical Properties
mp  124-126 °C(lit.)
density  1.285
CAS DataBase Reference 6484-25-9(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26
WGK Germany  3
 
 
4-CHLORO-2-PHENYLQUINAZOLINE Usage And Synthesis
Chemical Properties slightly yellow to yellow crystalline powder
Usage Reactnat involved in the synthesis of biologically active molecules including:• ;Nitrotriazole amines or nitroimidazole amines for use as antitrypanosomal activity and mammalian cytotoxicity1• ;Quinazoline-containing piperazinylpyrimidine derivatives with antitumor activity2• ;Quinazoline substituted cyclopentane as HCV NS3/4A protease inhibitors3• ;Quinazolines with antibacterial and antitumor activity4• ;Aurora inhibitor MK-04575Reactant involved in Suzuki-Miyaura cross-coupling6 and catalyst-free / base-free water promoted nucleophilic aromatic substitution7

 

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