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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)-

6-Chloro-2-(dimethylamino)nicotinaldehyde

O=Cc1ccc(nc1N(C)C)Cl Request for Quotation
Chemical Name: 6-Chloro-2-(dimethylamino)nicotinaldehyde
CAS Number: 1233698-83-3
Product Number: AG000KG4(AGN-PC-0WABWL)
Synonyms:
MDL No:
Molecular Formula: C8H9ClN2O
Molecular Weight: 184.6229

Identification/Properties

Computed Properties
Molecular Weight:
184.623g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
184.04g/mol
Monoisotopic Mass:
184.04g/mol
Topological Polar Surface Area:
33.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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


6-Chloro-2-(dimethylamino)nicotinaldehyde, known for its versatile properties, serves as a valuable intermediate in chemical synthesis. This compound plays a crucial role in the development of various organic compounds due to its unique structure and reactivity. In the realm of chemical synthesis, this aldehyde is particularly prized for its ability to undergo diverse reactions, enabling the creation of novel compounds with distinct functionalities. Whether employed as a key building block or a modifying agent, 6-Chloro-2-(dimethylamino)nicotinaldehyde facilitates the synthesis of complex molecules in a precise and efficient manner. Its compatibility with a wide range of reagents and catalysts further enhances its utility, making it an indispensable component in the toolbox of synthetic chemists striving to innovate and advance the field.