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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, 1-methyl-

NCC1(C)CC1 Request for Quotation
Chemical Name: Cyclopropanemethanamine, 1-methyl-
CAS Number: 98137-40-7
Product Number: AG00IK1B(AGN-PC-02YI69)
Synonyms:
MDL No:
Molecular Formula: C5H11N
Molecular Weight: 85.14754

Identification/Properties

Computed Properties
Molecular Weight:
85.15g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
85.089g/mol
Monoisotopic Mass:
85.089g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
55
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The [(1-methylcyclopropyl)methyl]amine compound, also known as MCM amine, is a versatile building block in chemical synthesis. It is widely utilized as an intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This amine group can undergo a range of reactions, including alkylation, acylation, and reductive amination, making it a valuable tool for designing complex molecular structures. Its unique structural features provide opportunities for stereochemical control and optimization of desired properties in target molecules. In addition, the MCM amine can act as a chiral auxiliary in asymmetric synthesis, enabling the preparation of enantiomerically pure compounds with high selectivity. Its versatility and reactivity make it a valuable asset in organic synthesis and drug discovery efforts.