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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)-

Cyclopropanecarboxylic acid, 1-(methylamino)-, hydrochloride

CNC1(CC1)C(=O)O.Cl Request for Quotation
Chemical Name: Cyclopropanecarboxylic acid, 1-(methylamino)-, hydrochloride
CAS Number: 99324-91-1
Product Number: AG00IK9H(AGN-PC-00N1PV)
Synonyms:
MDL No:
Molecular Formula: C5H10ClNO2
Molecular Weight: 151.5914

Identification/Properties

Computed Properties
Molecular Weight:
151.59g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
151.04g/mol
Monoisotopic Mass:
151.04g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
118
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1-(Methylamino)cyclopropanecarboxylic acid hydrochloride serves as a valuable building block in chemical synthesis due to its unique structural and reactivity properties. This compound is commonly utilized in the pharmaceutical industry for the development of drugs and other bioactive molecules. Its cyclopropane ring provides a rigid and sterically constrained framework, leading to the creation of complex molecular architectures with enhanced biological activity. Additionally, the presence of the methylamino group offers a versatile site for further functionalization, allowing for the introduction of different chemical groups to modulate the compound's physicochemical properties. As a key intermediate in organic synthesis, 1-(Methylamino)cyclopropanecarboxylic acid hydrochloride enables the construction of diverse molecular structures with potential applications in medicinal chemistry and material science.