- 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 |
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 |