1. Home
  2. 6-chloro-2-methylpyrimidine-4-carbaldehyde

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-methylpyrimidine-4-carbaldehyde

O=Cc1cc(Cl)nc(n1)C Request for Quotation
Chemical Name: 6-chloro-2-methylpyrimidine-4-carbaldehyde
CAS Number: 933702-42-2
Product Number: AG00IHKC(AGN-PC-0ALQEC)
Synonyms:
MDL No:
Molecular Formula: C6H5ClN2O
Molecular Weight: 156.5697

Identification/Properties

Computed Properties
Molecular Weight:
156.569g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
156.009g/mol
Monoisotopic Mass:
156.009g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
131
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


6-Chloro-2-methylpyrimidine-4-carbaldehyde is a versatile compound that finds wide application in chemical synthesis. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. The presence of the aldehyde group makes it a valuable intermediate for the synthesis of complex molecules through diverse chemical reactions.One of the primary uses of 6-Chloro-2-methylpyrimidine-4-carbaldehyde is in the formation of heterocyclic compounds, where it acts as a precursor for the introduction of functional groups or substitutions. Its reactivity allows for the modification of the pyrimidine ring system, enabling the creation of novel structures with potentially enhanced properties.Furthermore, this compound plays a crucial role in the synthesis of bioactive molecules due to its ability to participate in various coupling reactions, such as nucleophilic additions, condensations, and cycloadditions. By incorporating 6-Chloro-2-methylpyrimidine-4-carbaldehyde into synthetic pathways, chemists can access a diverse array of target compounds with desired pharmacological or biological activities.Overall, the strategic placement of the chloro and aldehyde functionalities in 6-Chloro-2-methylpyrimidine-4-carbaldehyde makes it an indispensable tool for chemists involved in drug discovery, material science, and other fields requiring the precise manipulation of molecular structures.