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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, N-(4-fluorophenyl)-

NNC(=S)Nc1ccc(cc1)F Request for Quotation
Chemical Name: Hydrazinecarbothioamide, N-(4-fluorophenyl)-
CAS Number: 330-94-9
Product Number: AG003K3R(AGN-PC-0JVOOZ)
Synonyms:
MDL No:
Molecular Formula: C7H8FN3S
Molecular Weight: 185.2219

Identification/Properties

Properties
MP:
171℃
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
185.22g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
185.042g/mol
Monoisotopic Mass:
185.042g/mol
Topological Polar Surface Area:
82.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
157
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:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P264-P270-P301+P310-P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-Fluorophenyl)hydrazinecarbothioamide, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique reactivity and functional group transformations. This compound serves as a valuable building block in the synthesis of various organic molecules and pharmaceuticals due to its ability to participate in a variety of reactions.One of the key applications of N-(4-Fluorophenyl)hydrazinecarbothioamide in chemical synthesis is its use as a precursor for the preparation of thiosemicarbazones. Thiosemicarbazones are important intermediates in organic synthesis and can be further modified to form diverse compounds with potential biological activities. The presence of the fluorophenyl group in N-(4-Fluorophenyl)hydrazinecarbothioamide allows for selective functionalization and leads to the development of new molecules with enhanced properties.Moreover, N-(4-Fluorophenyl)hydrazinecarbothioamide can also undergo condensation reactions to form hydrazones, which are key structures in medicinal chemistry and drug design. The versatility of this compound enables chemists to control the reactivity and selectivity of the reactions, making it a valuable tool in the synthesis of complex organic molecules.Overall, the application of N-(4-Fluorophenyl)hydrazinecarbothioamide in chemical synthesis showcases its importance in the creation of novel compounds with potential pharmaceutical, agricultural, and material science applications.