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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)-

1-chloro-3-fluoro-5-methylbenzene

Cc1cc(F)cc(c1)Cl Request for Quotation
Chemical Name: 1-chloro-3-fluoro-5-methylbenzene
CAS Number: 93857-90-0
Product Number: AG00GUPD(AGN-PC-0KNZRW)
Synonyms:
MDL No:
Molecular Formula: C7H6ClF
Molecular Weight: 144.5739

Identification/Properties

Properties
BP:
159.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
144.573g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
144.014g/mol
Monoisotopic Mass:
144.014g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
94.9
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#:
1993
Hazard Statements:
H226-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloro-3-fluoro-5-methylbenzene, also known as Chloro-fluoro-methylbenzene, is a versatile chemical compound commonly used in organic synthesis. Its unique structure and reactivity make it a valuable building block in the production of various compounds and materials. In chemical synthesis, 1-Chloro-3-fluoro-5-methylbenzene is utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its chlorine and fluorine substituents confer specific properties that are crucial for introducing desired functionalities into target molecules. Furthermore, 1-Chloro-3-fluoro-5-methylbenzene can undergo various reactions such as nucleophilic substitution, electrophilic aromatic substitution, and cross-coupling reactions, enabling chemists to create complex structures efficiently. Its presence in a reaction scheme can lead to the formation of diverse compounds with specific applications in the fields of medicine, agriculture, and materials science. Overall, 1-Chloro-3-fluoro-5-methylbenzene plays a significant role in advancing the field of chemical synthesis by providing chemists with a powerful tool to design and construct molecules with tailored properties and functions.