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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)-

4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide

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Chemical Name: 4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide
CAS Number: 915087-26-2
Product Number: AG00IGQI(AGN-PC-0WD2DK)
Synonyms:
MDL No: MFCD09909370
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
247.273g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
247.112g/mol
Monoisotopic Mass:
247.112g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
372
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


4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the production of various pharmaceuticals, agrochemicals, and fine chemicals.One key application of 4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide is in the formation of complex heterocyclic structures. By utilizing the cyano group and fluorine substituents, chemists can efficiently introduce additional functional groups and stereochemical elements into the target molecules. This compound is particularly valuable in the synthesis of bioactive compounds, where precise structural modifications are crucial for enhancing biological activity.Furthermore, the presence of the N-methylbenzamide moiety in 4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide allows for easy derivatization and further functionalization. This enables chemists to tailor the compound's properties and optimize its performance for specific applications. Overall, 4-((1-Cyanocyclobutyl)amino)-2-fluoro-N-methylbenzamide is a valuable tool in the toolkit of synthetic chemists for creating novel molecules with potential therapeutic or industrial significance.