1H-Pyrrolo[2,3-c]pyridine-2-methanol|882881-15-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-Pyrrolo[2,3-c]pyridine-2-methanol

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Chemical Name:	1H-Pyrrolo[2,3-c]pyridine-2-methanol
CAS Number:	882881-15-4
Product Number:	AG00IF1A(AGN-PC-00CUSL)
Synonyms:
MDL No:
Molecular Formula:	C8H8N2O
Molecular Weight:	148.1619

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

148.165g/mol

XLogP3:

0.1

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

148.064g/mol

Monoisotopic Mass:

148.064g/mol

Topological Polar Surface Area:

48.9A^2

Heavy Atom Count:

Formal Charge:

Complexity:

140

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H302-H317

Precautionary Statements:

P280-P305+P351+P338

Class:

N/A

Packing Group:

N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure

The compound 1H-Pyrrolo[2,3-c]pyridin-2-yl)methanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable tool in the creation of various organic compounds. $name$ can be utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its functional groups allow for easy manipulation and modification, enabling chemists to introduce specific functionalities or stereochemical elements into target molecules.In organic synthesis, $name$ can serve as a starting material for the preparation of heterocyclic compounds, which are prevalent in many biologically active molecules. Its inclusion in a synthetic route can lead to the formation of complex structures with diverse properties.Additionally, $name$ can participate in various reactions such as cross-coupling, cyclization, and oxidation, expanding its utility in the assembly of intricate molecular architectures. Its compatibility with different synthetic methodologies makes it a valuable asset in the toolkit of synthetic chemists striving to access novel compounds.Overall, the application of (1H-Pyrrolo[2,3-c]pyridin-2-yl)methanol in chemical synthesis opens up possibilities for the efficient construction of diverse molecules with potential applications in the fields of medicine, agriculture, materials science, and beyond.