1. Home
  2. Hydrazinecarboxamide, 2-[[4-(4-fluorophenoxy)phenyl]methylene]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Hydrazinecarboxamide, 2-[[4-(4-fluorophenoxy)phenyl]methylene]-

NC(=O)NN=Cc1ccc(cc1)Oc1ccc(cc1)F Request for Quotation
Chemical Name: Hydrazinecarboxamide, 2-[[4-(4-fluorophenoxy)phenyl]methylene]-
CAS Number: 181144-66-1
Product Number: AG0022PL(AGN-PC-076OBU)
Synonyms:
MDL No:
Molecular Formula: C14H12FN3O2
Molecular Weight: 273.2624

Identification/Properties

Computed Properties
Molecular Weight:
273.267g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
273.091g/mol
Monoisotopic Mass:
273.091g/mol
Topological Polar Surface Area:
76.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
335
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(4-(4-Fluorophenoxy)benzylidene)hydrazinecarboxamide is a versatile compound widely used in chemical synthesis due to its unique chemical structure and reactivity. This compound is commonly employed in the synthesis of various organic compounds and pharmaceuticals, functioning as a key intermediate in several important reactions.One of the primary applications of 2-(4-(4-Fluorophenoxy)benzylidene)hydrazinecarboxamide in chemical synthesis is as a building block for the preparation of heterocyclic compounds. By reacting this compound with different reagents or functional groups, chemists can access a diverse range of complex molecules with specific properties and functionalities.Additionally, 2-(4-(4-Fluorophenoxy)benzylidene)hydrazinecarboxamide can be utilized as a ligand in coordination chemistry, enabling the formation of coordination complexes with transition metals. These complexes exhibit unique reactivity and catalytic properties, making them valuable in various synthetic transformations.Overall, the versatility and utility of 2-(4-(4-Fluorophenoxy)benzylidene)hydrazinecarboxamide in chemical synthesis make it a valuable tool for researchers and chemists striving to access novel compounds and advance the field of organic chemistry.