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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)-

Benzaldehyde, 2,4,6-trichloro-

O=Cc1c(Cl)cc(cc1Cl)Cl Request for Quotation
Chemical Name: Benzaldehyde, 2,4,6-trichloro-
CAS Number: 24473-00-5
Product Number: AG002O96(AGN-PC-0LPXXF)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl3O
Molecular Weight: 209.4571

Identification/Properties

Properties
MP:
58.5-59.5℃
BP:
180-195℃ (12 Torr)
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
209.45g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
207.925g/mol
Monoisotopic Mass:
207.925g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
139
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


2,4,6-Trichlorobenzaldehyde, also known as TCBAL, is a versatile compound widely used in chemical synthesis. Its unique chemical structure makes it a valuable building block in the production of various organic compounds. TCBAL is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, dyes, and flavors.In organic synthesis, 2,4,6-Trichlorobenzaldehyde serves as a crucial starting material for the preparation of biologically active molecules. Its reactive aldehyde group allows for easy functionalization through various chemical reactions such as nucleophilic additions, condensations, and reductions. This flexibility makes TCBAL a preferred choice for creating complex molecular structures.Moreover, the presence of three chlorine atoms in TCBAL enhances its reactivity and selectivity in synthesis, enabling chemists to manipulate the properties and functions of the final products. The use of 2,4,6-Trichlorobenzaldehyde in chemical reactions contributes to the efficient and targeted formation of desired organic compounds with specific characteristics for diverse applications.