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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-Isoquinolinamine, 4-methyl-

Cc1cncc2c1c(N)ccc2 Request for Quotation
Chemical Name: 5-Isoquinolinamine, 4-methyl-
CAS Number: 194032-18-3
Product Number: AG00ACCN(AGN-PC-03IL0S)
Synonyms:
MDL No:
Molecular Formula: C10H10N2
Molecular Weight: 158.1998

Identification/Properties

Properties
BP:
351.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
158.204g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
158.084g/mol
Monoisotopic Mass:
158.084g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
158
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methylisoquinolin-5-amine, also known by its chemical formula C10H10N2, serves as a crucial building block in organic chemical synthesis. Due to its unique molecular structure, this compound finds widespread applications in the pharmaceutical and agrochemical industries.4-Methylisoquinolin-5-amine is primarily utilized as a key intermediate in the synthesis of various biologically active compounds. Its amino group provides a versatile site for functionalization, enabling the introduction of different substituents to tailor the properties of the final product. This compound is often employed in the development of novel pharmaceutical agents, particularly in the production of potential drugs for treating various diseases.Furthermore, 4-Methylisoquinolin-5-amine plays a vital role in the creation of specialized materials and organic dyes. Its structural characteristics contribute to the formation of complex molecules with specific properties, making it valuable for designing advanced materials with desired functionalities.In summary, the application of 4-Methylisoquinolin-5-amine in chemical synthesis extends across diverse fields, ranging from pharmaceuticals to materials science. Its synthesis and manipulation enable the production of a wide array of compounds with tailored properties and applications.