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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)-

2-N,2-N-dimethylpyridine-2,5-diamine;hydrochloride

Nc1ccc(nc1)N(C)C.Cl Request for Quotation
Chemical Name: 2-N,2-N-dimethylpyridine-2,5-diamine;hydrochloride
CAS Number: 119151-81-4
Product Number: AG000I9E(AGN-PC-0J0YBF)
Synonyms:
MDL No:
Molecular Formula: C7H12ClN3
Molecular Weight: 173.6433

Identification/Properties

Computed Properties
Molecular Weight:
173.644g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
173.072g/mol
Monoisotopic Mass:
173.072g/mol
Topological Polar Surface Area:
42.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
103
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, N2,N2-Dimethylpyridine-2,5-diamine hydrochloride plays a crucial role as a versatile reagent. Its unique structure and properties make it a valuable tool for various reactions and transformations in organic chemistry. This compound is commonly used as a catalyst or component in the synthesis of heterocyclic compounds, pharmaceuticals, and complex organic molecules. Its high reactivity and selectivity make it ideal for facilitating specific chemical reactions, such as N-alkylation, acylation, and oxidative processes. Furthermore, N2,N2-Dimethylpyridine-2,5-diamine hydrochloride's ability to participate in C-N bond formation and functional group interconversions make it a valuable asset in the toolbox of synthetic chemists looking to streamline and optimize their synthetic routes. Its applications extend across various industries, including drug discovery, materials science, and chemical manufacturing, highlighting its importance in advancing scientific research and innovation.