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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)-

ethyl 1-aminocyclopropane-1-carboxylate;hydrochloride

CCOC(=O)C1(N)CC1.Cl Request for Quotation
Chemical Name: ethyl 1-aminocyclopropane-1-carboxylate;hydrochloride
CAS Number: 42303-42-4
Product Number: AG0032OD(AGN-PC-0JQ0AJ)
Synonyms:
MDL No: MFCD00190747
Molecular Formula: C6H12ClNO2
Molecular Weight: 165.6180

Identification/Properties

Properties
MP:
108 - 110 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
165.617g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
165.056g/mol
Monoisotopic Mass:
165.056g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Amino-Cyclopropyl-1-Carboxylic Acid Ethyl Ester Hydrochloride, also known as $name$, is a versatile compound widely used in organic chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure and reactivity make it a valuable intermediate in the production of complex organic molecules.In chemical synthesis, $name$ can be employed as a precursor for the synthesis of heterocyclic compounds, which are essential in drug discovery and development. It can undergo various reactions such as acylation, alkylation, and cyclization to form new carbon-carbon and carbon-nitrogen bonds, enabling the construction of intricate molecular frameworks.Additionally, $name$ can be utilized in the preparation of peptide derivatives, which are crucial in the field of medicinal chemistry. By incorporating this compound into peptide synthesis strategies, chemists can access a diverse range of peptide analogs with enhanced bioactivity and pharmacokinetic properties.Furthermore, the hydrochloride salt form of 1-Amino-Cyclopropyl-1-Carboxylic Acid Ethyl Ester provides improved solubility and stability in aqueous solutions, facilitating its integration into various synthetic routes. Its compatibility with a wide range of reagents and reaction conditions makes it a valuable tool for organic chemists seeking to streamline the synthesis of complex organic molecules.In summary, the application of 1-Amino-Cyclopropyl-1-Carboxylic Acid Ethyl Ester Hydrochloride in chemical synthesis is instrumental in the creation of novel pharmaceuticals, agrochemicals, and fine chemicals. Its versatility and reactivity make it a valuable asset for organic chemists working in the field of drug discovery, medicinal chemistry, and materials science.