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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)-

4-chloro-8-fluoro-2-methylquinoline

Cc1cc(Cl)c2c(n1)c(F)ccc2 Request for Quotation
Chemical Name: 4-chloro-8-fluoro-2-methylquinoline
CAS Number: 18615-59-3
Product Number: AG003L64(AGN-PC-0NIJR9)
Synonyms:
MDL No:
Molecular Formula: C10H7ClFN
Molecular Weight: 195.6207

Identification/Properties

Properties
BP:
269.859°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
195.621g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
195.025g/mol
Monoisotopic Mass:
195.025g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
188
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:
Danger
UN#:
1759
Hazard Statements:
H302-H318
Precautionary Statements:
P264-P270-P280-P301+P312+P330-P305+P351+P338+P310-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-Chloro-8-fluoro-2-methylquinoline is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 4-Chloro-8-fluoro-2-methylquinoline serves as a key intermediate in the preparation of diverse organic compounds. Its substituted quinoline core provides a foundation for further modifications, allowing chemists to introduce specific functional groups or structural motifs with precision. This flexibility enables the fine-tuning of molecular properties and the development of novel compounds with tailored characteristics.The compound's chloro and fluoro substituents confer distinct chemical properties that can be leveraged in synthetic transformations. The chloro group, for instance, can undergo various nucleophilic substitution reactions, expanding the compound's synthetic utility. Meanwhile, the fluoro substituent can modulate the compound's reactivity and influence its interactions with other molecules, facilitating the design of new chemical entities with desired features.Overall, the use of 4-Chloro-8-fluoro-2-methylquinoline in chemical synthesis exemplifies its importance as a strategic building block for crafting sophisticated molecules with specific applications in various industries.