Interesting facts
Interesting Facts about 3,4-dihydro-1H-isoquinoline-2-carboxamidine
3,4-dihydro-1H-isoquinoline-2-carboxamidine is a fascinating compound that has piqued the interest of chemists due to its unique structure and potential applications. Below are key points that highlight its significance:
- Structural Features: This compound belongs to the isoquinoline family, characterized by its fused ring structure that contributes to its interesting chemical behavior. The presence of the "dihydro" prefix indicates that it has undergone hydrogenation, altering its reactivity.
- Biological Activity: Researchers are particularly interested in the biological implications of 3,4-dihydro-1H-isoquinoline derivatives. Some studies suggest that similar compounds have potential therapeutic applications, especially in the realms of neurology and pharmacology.
- Precursor for Synthesis: This compound is often regarded as a versatile precursor in organic synthesis, allowing chemists to create a variety of other complex molecules. Its ability to participate in further chemical reactions enhances its value in synthetic chemistry.
- Research Exploration: Current studies are exploring the role of derivatives of this compound in antioxidative and antimicrobial activities. The ongoing research may lead to the discovery of new therapeutic agents that could benefit medicine.
In summary, 3,4-dihydro-1H-isoquinoline-2-carboxamidine stands out not just for its chemical structure but also for its potential broad applications in scientific research. As the field of organic chemistry advances, compounds like this continue to be of great interest to scientists and researchers alike.
Synonyms
Debrisoquine
Debrisoquin
1131-64-2
Debrisochinum
Isocaramidine
Debrisoquina
3,4-dihydroisoquinoline-2(1H)-carboximidamide
Debrisoquinum
Debrisoquinum [INN-Latin]
Debrisoquina [INN-Spanish]
Debrisoquine [INN:BAN]
2(1H)-Isoquinolinecarboximidamide, 3,4-dihydro-
DEBRISOQUIN SULFATE
Declinax
Equitonil
Isocaramidine sulfate
EINECS 214-470-1
3,4-Dihydro-2(1H)-isoquinolinecarboxamidine
Debrisoquin hemisulfate
3,4-dihydro-1H-isoquinoline-2-carboximidamide
3,4-Dihydro-2(1H)-isoquinolinecarboximidamide
2(1H)-Isoquinolinecarboximidamide,3,4-dihydro-
CHEBI:34665
DEBRISOQUIN [MI]
DEBRISOQUINE [INN]
1,2,3,4-tetrahydroisoquinoline-2-carboximidamide
Debrisoquine; Isocaramidine
3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXAMIDINE
DEBRISOQUINE [WHO-DD]
CHEMBL169901
X31CDK040E
DTXSID7022885
Debrisoquinum (INN-Latin)
Debrisoquina (INN-Spanish)
Ro 5-3307/1
3,4-Dihydro-2(1H)-isoquinolinecarboxamidine sulfate (2:1)
NSC139330
SR-01000075159
NCGC00016513-01
CAS-581-88-4
UNII-X31CDK040E
3,4-Dihydro-2(1H)-isoquinoline carboxamidine sulfate
2(1H)-isoquinolinecarboximidamide, 3,4-dihydro-, sulfate (1:1)
2-Amidino-1,2,3,4-tetrahydroisoquinoline
Prestwick0_000372
Prestwick1_000372
Prestwick2_000372
Prestwick3_000372
Lopac0_000326
BSPBio_000523
SCHEMBL309184
SPBio_002444
BPBio1_000577
DTXCID202885
1,2,3, 4-Tetrahydro-isoquinoline-2-carboxamidine sulfate
C02CC04
HMS2089P09
2(1H)-Isoquinolinecarboxamidine, 3,4-dihydro-, sulfate (2:1)
ALBB-022123
BCP18785
HY-B1624
BDBM50122613
MSK159606
STK232096
AKOS000225362
BS-3952
DB04840
SDCCGSBI-0206944.P002
Sulfuric acid compound with 3,4-dihydro-2(1H)-isoquinolinecarboximidamide (1:1)
NCGC00016513-02
NCGC00016513-03
DA-69869
SBI-0206944.P001
1ST159606
CS-0013557
NS00003334
EN300-8045934
3,4-Dihydro-2(1H)-isoquinolinecarboximidamide #
Q3704421
SR-01000075159-1
SR-01000075159-4
BRD-K80419150-001-02-4
BRD-K80419150-065-03-7
2(1H)-Isoquinolinecarboxamidine, 3,4-dihydro- (7CI,8CI)
Solubility of 3,4-dihydro-1H-isoquinoline-2-carboxamidine
3,4-dihydro-1H-isoquinoline-2-carboxamidine, with the chemical formula C10H13N3, presents an intriguing case when it comes to solubility. Its solubility is affected by several factors, and it is essential to consider the following:
In summary, the solubility of C10H13N3 is largely determined by its chemical structure and environmental conditions. As highlighted, it is crucial to choose the appropriate solvent and consider temperature to achieve optimal solubility. Indeed, understanding these relationships can significantly aid in the practical applications of this compound in various fields.