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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-3-(4-chlorophenyl)propanoic acid

NC(c1ccc(cc1)Cl)CC(=O)O Request for Quotation
Chemical Name: 3-amino-3-(4-chlorophenyl)propanoic acid
CAS Number: 19947-39-8
Product Number: AG002C52(AGN-PC-0JMFYT)
Synonyms:
MDL No: MFCD00126370
Molecular Formula: C9H10ClNO2
Molecular Weight: 199.6342

Identification/Properties

Properties
MP:
223 °C (dec.)(lit.)
BP:
345.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5790 (estimate)
Computed Properties
Molecular Weight:
199.634g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
199.04g/mol
Monoisotopic Mass:
199.04g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


3-Amino-3-(4-Chlorophenyl)Propionic Acid, also known as 4-ACP, plays a crucial role in chemical synthesis as a versatile building block for various compounds. Its primary application lies in the field of pharmaceutical and medicinal chemistry, where it serves as a key intermediate in the synthesis of pharmaceutical compounds and drug molecules.In chemical synthesis, 3-Amino-3-(4-Chlorophenyl)Propionic Acid is often used as a starting material for the preparation of diverse organic compounds due to its unique structural properties. It can undergo various chemical reactions, such as acylation, amidation, and cyclization, to yield complex molecules with specific functionalities.One of the notable applications of 4-ACP is its use in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) such as Ibuprofen. By incorporating 3-Amino-3-(4-Chlorophenyl)Propionic Acid into the synthetic pathway, chemists can efficiently access pharmaceutical compounds that exhibit analgesic, anti-inflammatory, and antipyretic properties.Additionally, 4-ACP can also be utilized in the preparation of agrochemicals, fragrances, and other fine chemicals where its structural features can be tailored to impart desired biological or physicochemical properties to the final product. Its versatility and synthetic accessibility make it a valuable building block in the toolbox of organic chemists for creating diverse compounds of interest.