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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)-

cyclopropyl(pyridin-4-yl)methanamine

NC(c1ccncc1)C1CC1 Request for Quotation
Chemical Name: cyclopropyl(pyridin-4-yl)methanamine
CAS Number: 1270506-12-1
Product Number: AG000WMN(AGN-PC-03NL14)
Synonyms:
MDL No: MFCD18652126
Molecular Formula: C9H12N2
Molecular Weight: 148.2050

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
148.209g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
148.1g/mol
Monoisotopic Mass:
148.1g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
126
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

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


1-Cyclopropyl-1-(4-pyridyl)methylamine is a versatile chemical compound widely used in chemical synthesis as a valuable building block. Its unique structure containing both a cyclopropyl and a pyridyl moiety imparts special reactivity and functionality that make it a preferred choice in various synthetic routes. In organic synthesis, this compound serves as a key intermediate in the preparation of diverse pharmaceuticals, agrochemicals, and advanced materials. Due to its specific structural features, 1-Cyclopropyl-1-(4-pyridyl)methylamine can participate in a range of important reactions such as cross-coupling, nucleophilic substitution, and cyclization processes, offering chemists a valuable tool for constructing complex molecular architectures with precision and efficiency. Its application in chemical synthesis has been instrumental in the development of innovative molecules with potential therapeutic or industrial significance, making it an indispensable asset in modern synthetic chemistry endeavors.