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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)-

Cyclopropanecarboxamide, 1-bromo-

NC(=O)C1(Br)CC1 Request for Quotation
Chemical Name: Cyclopropanecarboxamide, 1-bromo-
CAS Number: 198758-97-3
Product Number: AG002BQ0(AGN-PC-039G3J)
Synonyms:
MDL No:
Molecular Formula: C4H6BrNO
Molecular Weight: 164.0005

Identification/Properties

Computed Properties
Molecular Weight:
164.002g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
162.963g/mol
Monoisotopic Mass:
162.963g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
108
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromocyclopropanecarboxamide is a versatile compound commonly used in chemical synthesis due to its unique reactivity and structural properties. As a reactive intermediate, it serves as a valuable building block in the synthesis of various organic compounds. Its three-membered cyclopropane ring imparts high strain energy, making it a powerful tool in organic transformations.In chemical synthesis, 1-Bromocyclopropanecarboxamide can undergo a variety of reactions, such as nucleophilic substitution, ring-opening reactions, and cross-coupling reactions, to produce complex molecules with diverse functionality. Its ability to participate in such reactions while maintaining the stability of the amide functional group makes it a valuable reagent for the construction of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, due to the presence of the bromine atom, 1-Bromocyclopropanecarboxamide can be easily modified to introduce different substituents or functional groups, providing chemists with a high degree of synthetic flexibility. This compound's unique combination of reactivity and stability makes it an essential component in the toolbox of synthetic chemists seeking to access novel structures and develop innovative chemical processes.