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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)-

(3R)-3-amino-3-cyclopropylpropanoic acid

NC(C1CC1)CC(=O)O Request for Quotation
Chemical Name: (3R)-3-amino-3-cyclopropylpropanoic acid
CAS Number: 331633-72-8
Product Number: AG003IUX(AGN-PC-05W1WN)
Synonyms:
MDL No: MFCD01861818
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
-2.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
120
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-3-cyclopropylpropanoic acid is a valuable compound widely utilized in chemical synthesis processes. This particular compound serves as a crucial building block in the creation of various pharmaceuticals and agrochemicals due to its versatile reactivity and unique structural properties. As a key intermediate, 3-Amino-3-cyclopropylpropanoic acid is often incorporated into the synthesis of complex molecules, enabling the introduction of essential functional groups while maintaining molecular stability. Its cyclopropyl ring imparts distinct stereochemical characteristics, making it a valuable component for designing chiral molecules in asymmetric synthesis. Additionally, the amino group present in the compound offers opportunities for further derivatization, allowing for the creation of diverse chemical entities with enhanced biological activities. In summary, the application of 3-Amino-3-cyclopropylpropanoic acid in chemical synthesis plays a pivotal role in the development of novel compounds with potential applications in pharmaceutical and agricultural industries.