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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)-

1H-Pyrrol-3-ol, 5-phenyl-

Oc1c[nH]c(c1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrrol-3-ol, 5-phenyl-
CAS Number: 100750-40-1
Product Number: AG0002TA(AGN-PC-0LAZ5F)
Synonyms:
MDL No:
Molecular Formula: C10H9NO
Molecular Weight: 159.1846

Identification/Properties

Computed Properties
Molecular Weight:
159.188g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
159.068g/mol
Monoisotopic Mass:
159.068g/mol
Topological Polar Surface Area:
36A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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


5-Phenyl-1H-pyrrol-3-ol, also known as phenylpyrrol, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely used in the pharmaceutical and agrochemical industries for the synthesis of various bioactive molecules and reaction intermediates. In organic chemistry, 5-Phenyl-1H-pyrrol-3-ol serves as a key starting material for the construction of diverse molecular structures due to its unique reactivity and ability to participate in a wide range of chemical transformations. Its functional group allows for the introduction of different substituents, enabling the creation of complex and valuable compounds with enhanced biological activities. Additionally, 5-Phenyl-1H-pyrrol-3-ol can serve as a scaffold for the development of novel drug candidates and functional materials through controlled modifications and chemical derivatization. Its versatile nature and synthetic utility make it a valuable tool for organic chemists seeking to explore new synthetic pathways and develop innovative molecules for various applications.