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Henan Tianfu Chemical Co., Ltd.4-CHLORO-2-PHENYLQUINAZOLINE//file1.lookchem.com/cas/reactions/2021/06/28/170938.png
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4-CHLORO-2-PHENYLQUINAZOLINE CAS NO.6484-25-9

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

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Product Details

Keywords

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

Quick Details

  • ProName: 4-CHLORO-2-PHENYLQUINAZOLINE
  • CasNo: 6484-25-9
  • Molecular Formula: C14H9ClN2
  • Appearance: slightly yellow to yellow crystalline ...
  • Application: For Organic Synthesis use
  • DeliveryTime: PROMPT
  • PackAge: IN 25kg drums
  • Port: SHANGHAI
  • ProductionCapacity: 10 Metric Ton/Month
  • Purity: 99.0%
  • Storage: In Room Temperature
  • Transportation: As Per MSDS
  • LimitNum: 1 Kilogram
  • Heavy metal: N/A
  • Grade: Industrial Grade,Food Grade,Pharma Gra...
  • Transportation: N/A

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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