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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-Chloro-2,4-difluorobenzylamine

NCc1cc(Cl)c(cc1F)F Request for Quotation
Chemical Name: 5-Chloro-2,4-difluorobenzylamine
CAS Number: 924818-16-6
Product Number: AG006HUT(AGN-PC-0WABA1)
Synonyms:
MDL No:
Molecular Formula: C7H6ClF2N
Molecular Weight: 177.5790

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;Keep in dry area;
Form:
Liquid
Computed Properties
Molecular Weight:
177.579g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
177.016g/mol
Monoisotopic Mass:
177.016g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
134
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(5-Chloro-2,4-difluorophenyl)methanamine is a versatile chemical compound that finds wide application in organic synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural properties. In chemical synthesis, (5-Chloro-2,4-difluorophenyl)methanamine can be utilized as a key intermediate in the production of complex molecules by participating in various reactions such as nucleophilic substitutions, reductive aminations, and cross-coupling reactions. Its presence enables the introduction of the 5-chloro-2,4-difluorophenyl functional group into target compounds, thus imparting specific characteristics and enhancing their biological or chemical activities. This compound's ability to act as a nucleophilic amine and undergo various transformations makes it a valuable tool for synthetic chemists seeking to access diverse chemical space and develop novel compounds with desired properties.