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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)-

3-Pyridinecarboxaldehyde, 2-chloro-5-methyl-

O=Cc1cc(C)cnc1Cl Request for Quotation
Chemical Name: 3-Pyridinecarboxaldehyde, 2-chloro-5-methyl-
CAS Number: 92444-99-0
Product Number: AG00GS2J(AGN-PC-0MUA3T)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO
Molecular Weight: 155.5816

Identification/Properties

Properties
BP:
265.511 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
155.581g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
155.014g/mol
Monoisotopic Mass:
155.014g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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#:
-
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-5-methylnicotinaldehyde, a fine chemical intermediate, plays a crucial role in chemical synthesis processes. Its unique chemical properties make it a valuable building block in the creation of various organic compounds. This compound serves as a versatile reagent in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. By utilizing 2-Chloro-5-methylnicotinaldehyde as a key component in reactions, chemists can efficiently access diverse molecular structures and functional groups, enabling the development of innovative and complex compounds for a wide range of applications.