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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)-

2-chloro-8-methylquinoline

Clc1ccc2c(n1)c(C)ccc2 Request for Quotation
Chemical Name: 2-chloro-8-methylquinoline
CAS Number: 4225-85-8
Product Number: AG00CAOY(AGN-PC-03CKYY)
Synonyms:
MDL No:
Molecular Formula: C10H8ClN
Molecular Weight: 177.6302

Identification/Properties

Computed Properties
Molecular Weight:
177.631g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
177.035g/mol
Monoisotopic Mass:
177.035g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
160
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:
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


2-Chloro-8-methylquinoline, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, 2-Chloro-8-methylquinoline plays a crucial role in the modification of aromatic rings to introduce functional groups that are essential for the development of new compounds with specific properties. Its unique structure and reactivity make it a valuable intermediate in the preparation of complex molecules by facilitating substitution, addition, and condensation reactions. Additionally, 2-Chloro-8-methylquinoline is utilized in the development of novel materials with specialized applications, such as dyes, pigments, and fluorescent probes. Its ability to undergo diverse chemical transformations enables researchers to tailor its properties for various purposes, making it a versatile tool in the field of chemical synthesis.