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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-pyrrolo[3,2-c]pyridine-3-carbaldehyde

O=Cc1c[nH]c2c1cncc2 Request for Quotation
Chemical Name: 1H-pyrrolo[3,2-c]pyridine-3-carbaldehyde
CAS Number: 933717-10-3
Product Number: AG00H01W(AGN-PC-01NI9M)
Synonyms:
MDL No:
Molecular Formula: C8H6N2O
Molecular Weight: 146.1460

Identification/Properties

Properties
BP:
383.175 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
146.149g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
146.048g/mol
Monoisotopic Mass:
146.048g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
160
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde in chemical synthesis is notably valuable in the field of organic chemistry due to its versatile reactivity and structural features. As a key intermediate in various synthetic pathways, this compound serves as a fundamental building block for the creation of diverse molecules with biological and pharmaceutical significance. Its unique heterocyclic structure makes it a pivotal component in the synthesis of complex compounds such as pharmaceuticals, agrochemicals, and materials. By participating in diverse chemical reactions, 1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde enables the efficient construction of structurally intricate molecules essential for advancing scientific research and industrial applications.