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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, 2,3,5-trichloro-

Clc1cc(O)c(c(c1)Cl)Cl Request for Quotation
Chemical Name: Phenol, 2,3,5-trichloro-
CAS Number: 933-78-8
Product Number: AG00GRS9(AGN-PC-0JKB9T)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl3O
Molecular Weight: 197.4464

Identification/Properties

Computed Properties
Molecular Weight:
197.439g/mol
XLogP3:
3.6
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335-H410
Precautionary Statements:
P261-P273-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,5-Trichlorophenol, also known as 2,3,5-TCP, is a versatile chemical compound widely used in chemical synthesis applications. With its unique molecular structure and reactivity, 2,3,5-TCP serves as a valuable building block for the synthesis of various organic compounds. In the realm of chemical synthesis, 2,3,5-Trichlorophenol is frequently employed as a precursor in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its trichloro-substituted phenolic ring provides a platform for the introduction of diverse functional groups through further chemical reactions. One common application of 2,3,5-TCP is in the synthesis of biologically active molecules, where its chlorinated phenolic moiety imparts specific properties and interactions necessary for the desired biological activity. Additionally, 2,3,5-Trichlorophenol can be utilized in the creation of intermediates for the synthesis of complex organic compounds.Due to its versatility and utility in chemical synthesis, 2,3,5-Trichlorophenol plays a crucial role in the development of new materials, pharmaceuticals, and other industrially important products. Its controlled use and manipulation in organic reactions make it a valuable tool for chemists and researchers seeking to design and create novel compounds for various applications.