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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)-

methyl 3-[(2-methylpropan-2-yl)oxycarbonylamino]furan-2-carboxylate

COC(=O)c1occc1NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: methyl 3-[(2-methylpropan-2-yl)oxycarbonylamino]furan-2-carboxylate
CAS Number: 956034-03-0
Product Number: AG006CCP(AGN-PC-09MQRE)
Synonyms:
MDL No:
Molecular Formula: C11H15NO5
Molecular Weight: 241.2405

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
241.243g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
241.095g/mol
Monoisotopic Mass:
241.095g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
297
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:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylate, commonly referred to as $name$, is a versatile compound that finds significant application in chemical synthesis. As a key building block in organic chemistry, $name$ is utilized in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ acts as a crucial intermediate for the preparation of complex molecules by enabling the introduction of the versatile furan and carbonyl functionalities into target compounds. The tert-butoxycarbonyl (Boc) protecting group on the amino functionality provides stability during reactions, allowing for selective transformations at other reactive sites within the molecule.Due to its structural attributes and reactivity, $name$ serves as a valuable tool in the synthesis of bioactive compounds, natural products, and functional materials. Its controlled manipulation in multistep syntheses enables chemists to streamline processes and access diverse chemical space for the development of novel molecules with desired properties.$name$ plays an essential role in the construction of molecular scaffolds and the modification of existing structures, making it indispensable in the field of medicinal chemistry, materials science, and chemical research. Its versatile nature and strategic positioning within synthetic routes make it an indispensable component in the toolbox of organic chemists seeking to access complex and valuable molecules efficiently.