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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)-

2-amino-3-(3-bromophenyl)propanoic acid

OC(=O)C(Cc1cccc(c1)Br)N Request for Quotation
Chemical Name: 2-amino-3-(3-bromophenyl)propanoic acid
CAS Number: 30163-20-3
Product Number: AG00I5NN(AGN-PC-0JSSOH)
Synonyms:
MDL No: MFCD05227935
Molecular Formula: C9H10BrNO2
Molecular Weight: 244.0852

Identification/Properties

Properties
MP:
206-210°C
BP:
368.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
244.088g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
242.989g/mol
Monoisotopic Mass:
242.989g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
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


2-Amino-3-(3-bromophenyl)propanoic acid, also known as $name$, serves as a versatile building block in chemical synthesis. This compound plays a crucial role in the creation of various synthetic molecules due to its unique structure and reactivity. One key application of 2-Amino-3-(3-bromophenyl)propanoic acid is its use as a precursor in the synthesis of pharmaceuticals and agrochemicals. By incorporating this compound into chemical reactions, chemists can introduce specific functional groups and stereochemical features into target molecules, allowing for the creation of new and potentially bioactive compounds. Additionally, 2-Amino-3-(3-bromophenyl)propanoic acid can be utilized in the preparation of advanced materials, such as polymers and catalysts, by serving as a key intermediate in multi-step synthetic pathways. Its versatility and importance in chemical synthesis make 2-Amino-3-(3-bromophenyl)propanoic acid a valuable tool for researchers and industry professionals seeking to develop innovative and complex molecular structures.