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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)-

Phenol, 2,3,6-trichloro-

Clc1ccc(c(c1Cl)O)Cl Request for Quotation
Chemical Name: Phenol, 2,3,6-trichloro-
CAS Number: 933-75-5
Product Number: AG003FFQ(AGN-PC-0JKB9S)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl3O
Molecular Weight: 197.4464

Identification/Properties

Properties
MP:
53-55℃ (lit.)
BP:
272 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
197.439g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
195.925g/mol
Monoisotopic Mass:
195.925g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
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-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,6-Trichlorophenol, also known as TCP, is a versatile compound widely utilized in chemical synthesis for various applications. In the field of organic chemistry, TCP is commonly employed as a building block in the synthesis of complex molecules and pharmaceuticals. Its unique chemical properties make it a valuable reagent for the formation of carbon-carbon and carbon-heteroatom bonds, essential for the creation of diverse chemical structures. Additionally, 2,3,6-Trichlorophenol is utilized in the production of pesticides, herbicides, and fungicides due to its effectiveness in inhibiting the growth of unwanted organisms. Its ability to undergo various chemical reactions under controlled conditions makes it a valuable tool in the hands of synthetic chemists, facilitating the creation of novel compounds with specific properties and applications.