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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)-

1H-Imidazo[4,5-c]quinoline, 4-chloro-1-(2-methylpropyl)-

CC(Cn1cnc2c1c1ccccc1nc2Cl)C Request for Quotation
Chemical Name: 1H-Imidazo[4,5-c]quinoline, 4-chloro-1-(2-methylpropyl)-
CAS Number: 99010-64-7
Product Number: AG006PJS(AGN-PC-0JPYVI)
Synonyms:
MDL No:
Molecular Formula: C14H14ClN3
Molecular Weight: 259.7341

Identification/Properties

Properties
MP:
141 - 142°C
BP:
427.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
259.737g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
259.088g/mol
Monoisotopic Mass:
259.088g/mol
Topological Polar Surface Area:
30.7A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
297
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline, also known by its chemical formula C₁₆H₁₇ClN₂, is a versatile compound widely utilized in chemical synthesis applications. This compound serves as a valuable building block in the creation of various organic molecules, thanks to its unique structure and reactivity.One of the key applications of 4-Chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline in chemical synthesis is its role as a precursor in the development of pharmaceutical compounds. Due to its ability to undergo diverse chemical transformations, this compound is frequently employed in the synthesis of novel drug candidates and bioactive molecules. Its chloro-substituted imidazoquinoline core provides a useful scaffold for the introduction of functional groups and modifications that are crucial for enhancing the desired biological activity of the final products.Furthermore, 4-Chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline is commonly used in the preparation of complex organic intermediates for the synthesis of agrochemicals, dyes, and materials with specific properties. Its structural features make it a valuable starting material for accessing a wide range of chemical structures through various synthetic routes, enabling the efficient production of target molecules with tailored properties and functionalities.In summary, the versatile nature and synthetic potential of 4-Chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline make it a valuable tool in chemical synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility and reactivity offer chemists the flexibility needed to design and prepare complex organic compounds with diverse applications and therapeutic potential.