1. Home
  2. 2,3-Pyridinediamine, 5,6-dichloro-

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)-

2,3-Pyridinediamine, 5,6-dichloro-

Nc1nc(Cl)c(cc1N)Cl Request for Quotation
Chemical Name: 2,3-Pyridinediamine, 5,6-dichloro-
CAS Number: 97941-89-4
Product Number: AG005XAH(AGN-PC-00MSIR)
Synonyms:
MDL No:
Molecular Formula: C5H5Cl2N3
Molecular Weight: 178.0193

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
178.016g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
176.986g/mol
Monoisotopic Mass:
176.986g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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


5,6-Dichloropyridine-2,3-diamine is a versatile compound commonly used in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique molecular structure allows it to participate in a wide range of reactions, making it a valuable tool for synthetic chemists.In chemical synthesis, 5,6-Dichloropyridine-2,3-diamine can be utilized in the production of heterocyclic compounds, which are essential in drug discovery and development. It can be employed as a key intermediate in the synthesis of complex organic molecules with diverse biological activities. Additionally, this compound can participate in coupling reactions to form C-N and C-C bonds, further expanding its utility in creating novel chemical entities.Furthermore, 5,6-Dichloropyridine-2,3-diamine is known for its reactivity towards various electrophiles and nucleophiles, allowing chemists to functionalize its structure in a controlled manner. This versatility makes it an indispensable tool in designing and synthesizing new compounds with tailored properties for specific applications in the pharmaceutical and agrochemical industries.