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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)-

5H-Pyrrolo[1,2-a]imidazol-7-ol, 6,7-dihydro-

OC1CCn2c1ncc2 Request for Quotation
Chemical Name: 5H-Pyrrolo[1,2-a]imidazol-7-ol, 6,7-dihydro-
CAS Number: 112513-79-8
Product Number: AG0039S4(AGN-PC-00O2RS)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O
Molecular Weight: 124.1405

Identification/Properties

Computed Properties
Molecular Weight:
124.143g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
124.064g/mol
Monoisotopic Mass:
124.064g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
118
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dihydro-5H-pyrrolo[1,2-a]imidazol-7-ol, commonly referred to as $name$, is a versatile compound extensively used in chemical synthesis. Due to its unique molecular structure, $name$ exhibits remarkable reactivity and serves as a key building block in the creation of various organic compounds.One of the prominent applications of $name$ in chemical synthesis is its role as a precursor in the synthesis of heterocyclic compounds. By utilizing $name$ as a starting material, chemists can readily introduce functional groups and modulate the chemical properties of the resulting molecules. This versatility allows for the synthesis of diverse organic compounds with tailored properties for specific applications in pharmaceuticals, materials science, and agrochemicals.$name$ also plays a crucial role in the development of pharmaceutical agents. Its inclusion in synthetic pathways enables the production of drug candidates with potent biological activities and enhanced pharmacokinetic profiles. Through strategic modifications of the $name$ moiety, chemists can fine-tune the medicinal properties of the final compounds, paving the way for the discovery of novel therapeutics.In addition, the presence of the pyrroloimidazol-ol core in $name$ imparts valuable structural characteristics that are advantageous for designing bioactive molecules. This structural motif has been exploited in the design of enzyme inhibitors, receptor modulators, and other biologically active compounds. The synthesis of these molecules often involves the strategic incorporation of $name$ to achieve the desired pharmacological effects.Overall, the strategic use of 6,7-Dihydro-5H-pyrrolo[1,2-a]imidazol-7-ol in chemical synthesis offers a wide array of possibilities for creating intricate organic compounds with tailored properties. Its importance as a versatile building block underscores its significance in the field of organic chemistry and drug discovery.