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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)-

Pyridine, 3,4,5-trichloro-

Clc1c(Cl)cncc1Cl Request for Quotation
Chemical Name: Pyridine, 3,4,5-trichloro-
CAS Number: 33216-52-3
Product Number: AG003IEE(AGN-PC-0L01VO)
Synonyms:
MDL No: MFCD00051685
Molecular Formula: C5H2Cl3N
Molecular Weight: 182.4351

Identification/Properties

Properties
MP:
75-77°C
BP:
209.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
182.428g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
180.925g/mol
Monoisotopic Mass:
180.925g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
88.2
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4,5-Trichloropyridine is a versatile compound commonly employed in chemical synthesis processes. As a building block in organic chemistry, this compound serves various applications in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex molecules.One key application of 3,4,5-Trichloropyridine is its role as a precursor in the manufacturing of herbicides and insecticides. It can undergo various chemical transformations to introduce functional groups that enhance the biological activity of the final products. Additionally, this compound is utilized in the synthesis of pharmaceutical compounds, particularly in the development of novel drugs with therapeutic properties.In chemical synthesis, 3,4,5-Trichloropyridine can participate in diverse reactions such as nucleophilic substitutions, cross-coupling reactions, and heterocyclic syntheses. Its ability to undergo selective modifications makes it a valuable tool for organic chemists in designing efficient routes to complex molecules. Furthermore, the presence of multiple chlorine atoms in the molecule can facilitate further derivatization to fine-tune the properties of the desired products.Overall, the use of 3,4,5-Trichloropyridine in chemical synthesis enables researchers and industrial chemists to access a wide range of structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.