1. Home
  2. Pyridine, 2-chloro-5-(trichloromethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, 2-chloro-5-(trichloromethyl)-

Clc1ccc(cn1)C(Cl)(Cl)Cl Request for Quotation
Chemical Name: Pyridine, 2-chloro-5-(trichloromethyl)-
CAS Number: 69045-78-9
Product Number: AG005M3Z(AGN-PC-0JKXM1)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl4N
Molecular Weight: 230.9067

Identification/Properties

Properties
MP:
53-55°C
BP:
281.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
230.897g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
230.899g/mol
Monoisotopic Mass:
228.902g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
133
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-5-(trichloromethyl)pyridine, also known as $name$, is a versatile chemical compound that finds wide application in organic synthesis. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. One of the key applications of 2-Chloro-5-(trichloromethyl)pyridine in chemical synthesis is as a reagent in the preparation of diverse heterocyclic compounds. It is commonly used as a precursor in the synthesis of pyridine derivatives, which are important structural motifs found in many biologically active molecules. Furthermore, 2-Chloro-5-(trichloromethyl)pyridine can be utilized as a key intermediate in the synthesis of herbicides and pesticides, where its unique structure imparts desirable biological activity. Its trichloromethyl group can enhance the potency and selectivity of the final compounds, making it an indispensable component in the development of agricultural chemicals.In addition, this compound can participate in various functional group transformations and cross-coupling reactions, allowing for the introduction of diverse chemical functionalities into complex molecular structures. Its versatile reactivity and compatibility with a wide range of reaction conditions make it a valuable tool for synthetic chemists in achieving molecular diversity and complexity in their target molecules.