1. Home
  2. 3-Pyridinamine, 2,4-dichloro-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

3-Pyridinamine, 2,4-dichloro-

Nc1c(Cl)ccnc1Cl Request for Quotation
Chemical Name: 3-Pyridinamine, 2,4-dichloro-
CAS Number: 173772-63-9
Product Number: AG001Z67(AGN-PC-0MUMTD)
Synonyms:
MDL No: MFCD09750301
Molecular Formula: C5H4Cl2N2
Molecular Weight: 163.0047

Identification/Properties

Computed Properties
Molecular Weight:
163.001g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
161.975g/mol
Monoisotopic Mass:
161.975g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Amino-2,4-dichloropyridine is a versatile compound that finds numerous applications in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to participate in a wide range of reactions, making it a valuable intermediate in organic synthesis.In chemical synthesis, 3-Amino-2,4-dichloropyridine can be utilized in the preparation of heterocyclic compounds, which are essential components in the development of new drugs and agricultural chemicals. By reacting with different reagents, this compound can undergo various functional group transformations, leading to the formation of diverse molecular structures with desired properties.Moreover, 3-Amino-2,4-dichloropyridine can be employed in the modification of existing molecules to enhance their biological or chemical activities. Through selective derivatization reactions, researchers can fine-tune the characteristics of a compound to improve its efficacy or selectivity in specific applications.Overall, the use of 3-Amino-2,4-dichloropyridine in chemical synthesis enables chemists to access a wide array of functionalized pyridine derivatives, opening up opportunities for the development of novel compounds with potential therapeutic, agricultural, or industrial significance.