Identification |
Name: | Quinazoline,4-chloro-2-phenyl- |
Synonyms: | 2-Phenyl-4-chloroquinazoline;4-Chloro-2-phenylquinazoline; NSC 400965 |
CAS: | 6484-25-9 |
EINECS: | 229-346-2 |
Molecular Formula: | C14H9 Cl N2 |
Molecular Weight: | 240.6877 |
InChI: | InChI=1/C14H9ClN2/c15-13-11-8-4-5-9-12(11)16-14(17-13)10-6-2-1-3-7-10/h1-9H |
Molecular Structure: |
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Properties |
Melting Point: | 124-126 °C(lit.) |
Flash Point: | 164.4°C |
Boiling Point: | 301.2°Cat760mmHg |
Density: | 1.285g/cm3 |
Refractive index: | 1.667 |
Appearance: | slightly yellow to yellow crystalline powder |
Specification: | slightly yellow to yellow crystalline powder usageEng: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 Safety Statements:37/39-26 37/39:Wear suitable protective clothing, gloves and eye/face
protection 26:In case of contact with eyes, rinse immediately with plenty
of water and seek medical advice |
Flash Point: | 164.4°C |
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 |
Safety Data |
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