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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)-

(3-amino-4-fluorophenyl) acetate

CC(=O)Oc1ccc(c(c1)N)F Request for Quotation
Chemical Name: (3-amino-4-fluorophenyl) acetate
CAS Number: 196610-38-5
Product Number: AG00I3KT(AGN-PC-0BICSE)
Synonyms:
MDL No:
Molecular Formula: C8H8FNO2
Molecular Weight: 169.1530

Identification/Properties

Computed Properties
Molecular Weight:
169.155g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
169.054g/mol
Monoisotopic Mass:
169.054g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
174
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-4-fluorophenyl acetate is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its amino and fluorine functional groups make it an ideal precursor for the synthesis of heterocyclic compounds and complex organic molecules with potentially beneficial biological activities. Additionally, 3-Amino-4-fluorophenyl acetate is commonly employed as a key intermediate in the production of specialty polymers and advanced materials. Its strategic position in the synthesis of diverse chemical compounds highlights its significance in modern synthetic chemistry.