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
0TO
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:
In general, its solubility behavior could be summarized as follows:
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.