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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)-

Benzenamine, 4-fluoro-N-(1-methylethyl)-

CC(Nc1ccc(cc1)F)C Request for Quotation
Chemical Name: Benzenamine, 4-fluoro-N-(1-methylethyl)-
CAS Number: 70441-63-3
Product Number: AG00F9U6(AGN-PC-0JPJWY)
Synonyms:
MDL No:
Molecular Formula: C9H12FN
Molecular Weight: 153.1967

Identification/Properties

Computed Properties
Molecular Weight:
153.2g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
153.095g/mol
Monoisotopic Mass:
153.095g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
106
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


4-Fluoro-N-isopropylaniline is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block for the preparation of various organic molecules, particularly in the pharmaceutical and agrochemical industries. Its unique structure and reactivity make it a key intermediate in the synthesis of complex compounds. Additionally, 4-Fluoro-N-isopropylaniline can be used as a precursor for the synthesis of dyes, polymers, and other specialty chemicals, showcasing its importance in a range of industries. Its compatibility with a variety of reaction conditions and ability to undergo functional group transformations make it a valuable tool for synthetic chemists seeking to access diverse chemical structures.