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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)-

Hydrazinecarbothioamide, 2-[(3-nitro-2-pyridinyl)methylene]-, (E)-

NC(=S)N/N=C/c1ncccc1[N+](=O)[O-] Request for Quotation
Chemical Name: Hydrazinecarbothioamide, 2-[(3-nitro-2-pyridinyl)methylene]-, (E)-
CAS Number: 200933-26-2
Product Number: AG002D3U(AGN-PC-0O7273)
Synonyms:
MDL No:
Molecular Formula: C7H7N5O2S
Molecular Weight: 225.2278

Identification/Properties

Computed Properties
Molecular Weight:
225.226g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
225.032g/mol
Monoisotopic Mass:
225.032g/mol
Topological Polar Surface Area:
141A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
277
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (E)-2-((3-Nitropyridin-2-yl)methylene)hydrazinecarbothioamide, when used in chemical synthesis, serves as a key reagent for the formation of various heterocyclic structures. Its unique chemical properties make it a versatile building block in the creation of pharmaceuticals, agrochemicals, and advanced materials. By participating in condensation reactions with suitable carbonyl compounds, this compound facilitates the generation of new carbon-nitrogen bonds, leading to the synthesis of diverse compounds with potential biological activities or functional properties. Furthermore, its ability to undergo substitution reactions enhances its applicability in the modification of organic molecules, offering opportunities for the design and creation of novel chemical entities with tailored properties.