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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)-

Benzenemethanamine, 2-chloro-4-fluoro-

NCc1ccc(cc1Cl)F Request for Quotation
Chemical Name: Benzenemethanamine, 2-chloro-4-fluoro-
CAS Number: 15205-11-5
Product Number: AG00337W(AGN-PC-0JMR07)
Synonyms:
MDL No: MFCD00042532
Molecular Formula: C7H7ClFN
Molecular Weight: 159.5886

Identification/Properties

Properties
MP:
172-173℃(Solv: N,N-dimethylformamide (68-12-2))
BP:
216.199°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Air Sensitive
Refractive Index:
1.535
Computed Properties
Molecular Weight:
159.588g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
159.025g/mol
Monoisotopic Mass:
159.025g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


2-Chloro-4-Fluorobenzylamine, also known by its chemical formula C7H7ClFN, is a crucial building block in chemical synthesis. Its application in organic chemistry lies in its functionality as a versatile intermediate for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Due to the presence of both a chlorine and a fluorine atom on the benzene ring, 2-Chloro-4-Fluorobenzylamine serves as a valuable starting material for creating more complex molecules through substitution reactions. These halogen atoms can be strategically manipulated to introduce other functional groups, thereby enabling the formation of diverse compounds with desired properties.The reactivity of 2-Chloro-4-Fluorobenzylamine makes it a preferred choice in the production of biologically active compounds and materials used in the pharmaceutical industry. Its incorporation into the chemical synthesis process facilitates the development of new drug candidates, insecticides, herbicides, and other specialty chemicals.Additionally, this compound's utility extends to the preparation of advanced building blocks for organic synthesis, allowing chemists to access a wide array of structurally diverse molecules. By carefully designing synthetic routes involving 2-Chloro-4-Fluorobenzylamine, researchers can efficiently construct complex molecular architectures with specific properties and functions.