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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)-

(2S)-2-pyrrol-1-ylpropanoic acid

CC(n1cccc1)C(=O)O Request for Quotation
Chemical Name: (2S)-2-pyrrol-1-ylpropanoic acid
CAS Number: 63751-72-4
Product Number: AG00EBZ3(AGN-PC-0JVBD6)
Synonyms:
MDL No:
Molecular Formula: C7H9NO2
Molecular Weight: 139.1519

Identification/Properties

Computed Properties
Molecular Weight:
139.154g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
139.063g/mol
Monoisotopic Mass:
139.063g/mol
Topological Polar Surface Area:
42.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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

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


2-(1H-Pyrrol-1-yl)propanoic acid is a versatile compound commonly used in chemical synthesis as a building block for various organic molecules. With its unique structure incorporating a pyrrole ring, this compound offers a range of applications in the synthesis of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-(1H-Pyrrol-1-yl)propanoic acid serves as a key intermediate for the production of heterocyclic compounds, which are prevalent in drug discovery and development. Its ability to participate in diverse reactions allows for the formation of complex molecular structures with potential biological activity.Furthermore, the pyrrole moiety in this acid provides opportunities for the introduction of functional groups and modifications, enabling chemists to tailor the properties of the final products. This flexibility makes 2-(1H-Pyrrol-1-yl)propanoic acid a valuable tool in designing and preparing novel compounds for various applications.Overall, the use of 2-(1H-Pyrrol-1-yl)propanoic acid in chemical synthesis showcases its significance in the creation of sophisticated organic molecules with potential therapeutic, agricultural, or material-based benefits.