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Cl-Quinazolin-4-amine

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Identification
Molecular formula
C17H14ClN3O2
CAS number
82916-45-2
IUPAC name
N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine
State
State

This compound is typically in a solid state at room temperature. It is stable under normal conditions but should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
177.50
Melting point (Kelvin)
450.65
Boiling point (Celsius)
333.20
Boiling point (Kelvin)
606.35
General information
Molecular weight
327.76g/mol
Molar mass
327.7620g/mol
Density
1.3571g/cm3
Appearence

N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine appears as a crystalline solid with a slightly yellowish tint. The crystals can be needle-like or plate-like depending on the method of synthesis and purification.

Comment on solubility

Solubility of N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine

The solubility of N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine (C17H14ClN3O2) can be influenced by several factors, including its structural characteristics and the solvent used.

Key Points on Solubility:

  • It is essential to consider polarity: The presence of methoxy groups (–OCH3) increases hydrophilicity, potentially aiding in solubility in polar solvents.
  • The incorporation of the chloro substituent may introduce steric hindrance that can affect the overall solubility in various media.
  • Primary solvents like ethanol and DMSO may be effective due to their ability to solvate both polar and non-polar sections of the molecule.

In general, its solubility behavior could be summarized as follows:

  1. Expected to show moderate to high solubility in polar organic solvents.
  2. Limited solubility in non-polar solvents due to the presence of polar functional groups.
  3. May exhibit variations in solubility based on the pH of the solution, particularly if it forms ionizable species.

Understanding the solubility of this compound is critical for its application in various chemical processes and pharmaceutical formulations. As a general guide, the more polar the solvent, the better the solubility of this compound is likely to be.

Interesting facts

Exploring N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine

N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine is a fascinating compound with a rich potential in medicinal chemistry. Here are some intriguing facts about this molecule:

  • Pharmacological Potential: This compound belongs to the quinazoline family, which is known for its various biological activities. Quinazolines have been reported to possess antitumor, antiviral, and antimicrobial properties.
  • Chlorine Substitution: The presence of the 3-chloro group on the phenyl ring greatly influences the compound's electronic properties, enhancing its ability to interact with biological targets.
  • Methoxy Groups: The dimethoxy substituents at positions 6 and 7 are known to contribute to the lipophilicity of the compound, affecting its absorption and distribution in biological systems.
  • Structure-Activity Relationship (SAR): Understanding how different substituents, like the chlorine and methoxy groups, alter the compound's efficacy is critical in drug design. It provides insights into optimizing therapeutic agents.
  • Pivotal in Research: Compounds like this serve as key intermediates for synthesizing more complex molecules, making them valuable in ongoing research for developing new drugs.

In summary, N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine showcases the intricate balance of chemical structure and biological function. Such compounds are essential in the search for new therapeutic agents that can combat various diseases.

Synonyms
153436-53-4
AG-1478
Tyrphostin AG 1478
N-(3-chlorophenyl)-6,7-dimethoxyquinazolin-4-amine
175178-82-2
Tyrphostin AG-1478
4-(3-Chloroanilino)-6,7-dimethoxyquinazoline
4-Quinazolinamine, N-(3-chlorophenyl)-6,7-dimethoxy-
AG1478
AG-1478 (Tyrphostin AG-1478)
tyrphostin AG1478
AG-1478 free base
SUH0SEZ9HY
MFCD00270914
TYRPHOSTIN
NSC-693255
CHEMBL7917
N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinamine
DTXSID0051447
CHEBI:75404
Tyrphostin AG-1478;NSC 693255
(3-Chlorophenyl)(6,7-dimethoxyquinazolin-4-yl)amine
BRD6408
Tyrphostins
BRD-6408
SR-01000076156
NSC693255
Tocris-1276
tyrphostin-AG-1478
UNII-SUH0SEZ9HY
InSolution AG 1478
BiomolKI_000018
Maybridge1_004001
Lopac-T-4182
BiomolKI2_000028
CBiol_002058
Lopac0_001127
Oprea1_653581
SCHEMBL93838
BSPBio_001390
KBioGR_000110
KBioSS_000110
MLS006012026
BDBM3532
GTPL4862
N-(3-chlorophenyl)-6,7-dimethoxy-quinazolin-4-amine
DTXCID9030044
BCBcMAP01_000035
HMS552N19
KBio2_000110
KBio2_002678
KBio2_005246
KBio3_000219
KBio3_000220
Bio1_000344
Bio1_000833
Bio1_001322
Bio2_000110
Bio2_000590
GLXC-04849
HMS1361F12
HMS1791F12
HMS1989F12
HMS3229O03
HMS3263B15
HMS3656B19
HMS3672E11
AHA17882
BCP07988
BCP15152
EX-A1236
Tyrphostin AG 1478, >=98%
Tox21_303781
Tox21_501127
BBL101047
CCG-52663
s2728
STL554841
AKOS002350880
CS-1606
LP01127
SB19361
SDCCGSBI-0051095.P003
SDCCGSBI-0051095.P008
IDI1_033860
NCGC00016017-01
NCGC00016017-02
NCGC00016017-03
NCGC00016017-04
NCGC00016017-05
NCGC00016017-06
NCGC00016017-07
NCGC00016017-08
NCGC00016017-09
NCGC00016017-20
NCGC00025093-01
NCGC00025093-02
NCGC00025093-03
NCGC00025093-04
NCGC00025093-05
NCGC00261812-01
NCGC00357072-01
AC-32828
GK 03499
HY-13524
NCI60_033425
SMR001456495
DB-026463
CAS-175178-82-2
EU-0101127
NS00017849
SW219714-1
T2944
6,7-dimethoxy-4-(3'-chloroanilino)quinazoline
T 4182
11N-812
AG-1478;Tyrphostin AG-1478; NSC 693255
CU-00000000399-1
SR-01000076156-1
SR-01000076156-4
SR-01000076156-7
AG 1478 - CAS 175178-82-2
BRD-K68336408-001-02-6
BRD-K68336408-001-10-9
BRD-K68336408-003-02-2
Q27074338
COC1=C(OC)C=C2C(NC3=CC(Cl)=CC=C3)=NC=NC2=C1
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