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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)-

Benzenemethanol, 2,4,6-trichloro-

OCc1c(Cl)cc(cc1Cl)Cl Request for Quotation
Chemical Name: Benzenemethanol, 2,4,6-trichloro-
CAS Number: 217479-60-2
Product Number: AG003FMS(AGN-PC-0LDNO7)
Synonyms:
MDL No:
Molecular Formula: C7H5Cl3O
Molecular Weight: 211.4730

Identification/Properties

Properties
MP:
98-101°C(lit.);
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
211.466g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
209.941g/mol
Monoisotopic Mass:
209.941g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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-Trichlorobenzyl alcohol is a versatile compound widely used in chemical synthesis as a key intermediate. Its primary application lies in organic chemistry, where it serves as a crucial building block for the synthesis of various compounds. Due to its unique chemical structure and reactivity, 2,4,6-Trichlorobenzyl alcohol is commonly employed in the pharmaceutical industry for the production of active pharmaceutical ingredients (APIs) and drug candidates. Additionally, this compound finds utility in the synthesis of agrochemicals, dyes, and other fine chemicals, highlighting its significance in modern chemical research and development. Its ability to undergo diverse chemical reactions and functional group transformations makes it a valuable tool for synthetic chemists seeking to access complex molecular architectures efficiently and selectively.