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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)-

3-Hydrazinyl-2-methylpyridineDihydrochloride

NNc1cccnc1C.Cl.Cl Request for Quotation
Chemical Name: 3-Hydrazinyl-2-methylpyridineDihydrochloride
CAS Number: 1803601-87-7
Product Number: AG00IM96(AGN-PC-0WAM7A)
Synonyms:
MDL No: MFCD26937550
Molecular Formula: C6H11Cl2N3
Molecular Weight: 196.0776

Identification/Properties

Computed Properties
Molecular Weight:
196.075g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
195.033g/mol
Monoisotopic Mass:
195.033g/mol
Topological Polar Surface Area:
50.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
84.4
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 3-Hydrazinyl-2-methylpyridine dihydrochloride is a versatile compound widely utilized in chemical synthesis for various applications. Its unique structure and properties make it a valuable reagent in the development of novel organic compounds. One of the key applications of 3-Hydrazinyl-2-methylpyridine dihydrochloride in chemical synthesis is as a building block in the preparation of heterocyclic compounds. This compound can undergo a variety of reactions, such as nucleophilic addition and condensation, to generate diverse heterocycles with potential biological activities. Its ability to participate in selective functional group transformations makes it a valuable tool for the synthesis of complex molecules.Furthermore, 3-Hydrazinyl-2-methylpyridine dihydrochloride can also serve as a catalyst in certain organic reactions. Its presence can facilitate the conversion of substrates into desired products with improved efficiency and selectivity. This catalytic activity opens up new possibilities for designing greener and more sustainable synthetic routes.In addition, the compound's hydrazine moiety enables it to act as a precursor for the introduction of nitrogen-containing functional groups in target molecules. This feature is particularly useful in medicinal chemistry and material science, where nitrogen-containing compounds are prevalent and play crucial roles in determining the properties and activities of the final products.Overall, the 3-Hydrazinyl-2-methylpyridine dihydrochloride is a valuable reagent in chemical synthesis, offering a wide range of applications in the construction of diverse organic compounds with potential utility in various fields.