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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)-

Cyclopropanemethanamine, a-methyl-, hydrochloride, (S)-

C[C@@H](C1CC1)N.Cl Request for Quotation
Chemical Name: Cyclopropanemethanamine, a-methyl-, hydrochloride, (S)-
CAS Number: 178033-78-8
Product Number: AG0039ZH(AGN-PC-0QB80O)
Synonyms:
MDL No:
Molecular Formula: C5H12ClN
Molecular Weight: 121.6085

Identification/Properties

Computed Properties
Molecular Weight:
121.608g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
121.066g/mol
Monoisotopic Mass:
121.066g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
47.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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 (S)-1-Cyclopropylethan-1-amine hydrochloride is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound is particularly valuable in asymmetric synthesis, where the chirality of the cyclopropyl group plays a crucial role in determining the stereochemistry of the final product.In organic chemistry, (S)-1-Cyclopropylethan-1-amine hydrochloride is commonly employed as a chiral building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its cyclopropyl moiety serves as a rigid and sterically demanding unit, enabling precise control over the stereochemical outcome of reactions.One of the key applications of (S)-1-Cyclopropylethan-1-amine hydrochloride is in the synthesis of chiral amines, which are essential structural motifs in many biologically active compounds. By incorporating this compound into the synthetic sequence, chemists can access enantiomerically pure molecules with high selectivity and efficiency.Furthermore, (S)-1-Cyclopropylethan-1-amine hydrochloride can also serve as a valuable starting material for the preparation of complex natural products and functional materials. Its versatile nature and compatibility with a wide range of synthetic transformations make it a valuable tool for the construction of diverse chemical structures with high stereochemical precision.