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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)-

1-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]hydrazine

CN(c1ccc(cn1)C(F)(F)F)N Request for Quotation
Chemical Name: 1-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]hydrazine
CAS Number: 163620-24-4
Product Number: AG001U9Y(AGN-PC-0KKYH1)
Synonyms:
MDL No:
Molecular Formula: C7H8F3N3
Molecular Weight: 191.1537

Identification/Properties

Computed Properties
Molecular Weight:
191.157g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
191.067g/mol
Monoisotopic Mass:
191.067g/mol
Topological Polar Surface Area:
42.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
171
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1-Methylhydrazinyl)-5-(trifluoromethyl)pyridine is a versatile compound widely utilized in chemical synthesis due to its unique properties. This organic compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoromethyl and hydrazine functional groups make it an ideal candidate for reactions involving nucleophilic additions, alkylations, and condensations.In chemical synthesis, 2-(1-Methylhydrazinyl)-5-(trifluoromethyl)pyridine is commonly employed as a key intermediate in the preparation of biologically active compounds, such as insecticides, herbicides, and pharmaceuticals. The trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, making it attractive for drug development purposes. Moreover, the presence of the hydrazine moiety allows for selective functionalization through various reactions, including acylation, alkylation, and cross-coupling reactions.Due to its unique combination of functional groups and reactivity, 2-(1-Methylhydrazinyl)-5-(trifluoromethyl)pyridine plays a crucial role in the synthesis of complex molecules with diverse applications in the chemical industry. Its versatile nature and compatibility with a wide range of synthetic methodologies make it a valuable tool for organic chemists seeking to access novel chemical structures with tailored properties.