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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)-

2-chloro-6-(trifluoromethyl)pyridine-3-carbaldehyde

O=Cc1ccc(nc1Cl)C(F)(F)F Request for Quotation
Chemical Name: 2-chloro-6-(trifluoromethyl)pyridine-3-carbaldehyde
CAS Number: 944900-06-5
Product Number: AG00H6CY(AGN-PC-07XUP7)
Synonyms:
MDL No:
Molecular Formula: C7H3ClF3NO
Molecular Weight: 209.5530

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
209.552g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
208.986g/mol
Monoisotopic Mass:
208.986g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
197
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

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Chemical Structure


2-Chloro-6-(trifluoromethyl)nicotinaldehyde is a versatile compound widely utilized in chemical synthesis. Its unique chemical properties make it a valuable building block in the creation of various organic compounds. 
This aldehyde derivative has found application in the development of pharmaceuticals, agrochemicals, and advanced materials. By serving as a key intermediate in the synthesis of complex molecules, 2-Chloro-6-(trifluoromethyl)nicotinaldehyde enables chemists to access a diverse range of structurally intricate compounds. Its incorporation in organic reactions allows for the introduction of specific functional groups and substitution patterns, enhancing the efficiency and precision of chemical transformations.  
Additionally, this compound's trifluoromethyl group confers desirable properties such as enhanced metabolic stability and altered physicochemical characteristics, making it an attractive candidate for drug discovery and material science research. In summary, the strategic use of 2-Chloro-6-(trifluoromethyl)nicotinaldehyde in chemical synthesis opens up opportunities for the development of novel compounds with diverse applications in various industries.