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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)-

2-Furancarboxamide, tetrahydro-

NC(=O)C1CCCO1 Request for Quotation
Chemical Name: 2-Furancarboxamide, tetrahydro-
CAS Number: 91470-28-9
Product Number: AG003UOX(AGN-PC-007OCU)
Synonyms:
MDL No: MFCD03929553
Molecular Formula: C5H9NO2
Molecular Weight: 115.1305

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
115.132g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
115.063g/mol
Monoisotopic Mass:
115.063g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
103
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
1325
Hazard Statements:
H228
Precautionary Statements:
P210-P240-P241-P280-P370+P378
Class:
4.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tetrahydrofuran-2-carboxamide, also known as THF-2-carboxamide, is a versatile organic compound used in various chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, THF-2-carboxamide is commonly employed as a reagent for the formation of amide bonds, a crucial step in the production of complex organic molecules. Its unique structure and properties make it a valuable tool for researchers and chemists working in fields such as medicinal chemistry, materials science, and drug discovery. Additionally, THF-2-carboxamide can function as a solvent, facilitating reactions and promoting efficient product formation in synthetic processes. With its broad applicability and utility in chemical synthesis, THF-2-carboxamide plays a significant role in advancing scientific research and innovation across various industries.