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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)-

Bicyclo[2.2.1]hept-5-ene-2-methanamine

NCC1CC2CC1C=C2 Request for Quotation
Chemical Name: Bicyclo[2.2.1]hept-5-ene-2-methanamine
CAS Number: 95-10-3
Product Number: AG003A70(AGN-PC-00HXQC)
Synonyms:
MDL No:
Molecular Formula: C8H13N
Molecular Weight: 123.1955

Identification/Properties

Computed Properties
Molecular Weight:
123.199g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
123.105g/mol
Monoisotopic Mass:
123.105g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
140
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
3
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:
Danger
UN#:
2735
Hazard Statements:
H227-H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bicyclo[2.2.1]hept-5-en-2-ylmethanamine is a versatile compound commonly employed in chemical synthesis for its unique structural properties and reactivity. Due to the bicyclic nature of its core ring system, this compound serves as a valuable building block in organic chemistry, enabling the synthesis of various complex molecules through strategic functional group manipulations. In particular, the presence of the amino group provides a crucial site for further derivatization, allowing for the introduction of different functional groups to tailor the compound for specific applications. This attribute makes Bicyclo[2.2.1]hept-5-en-2-ylmethanamine an indispensable intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals, where precise control over the molecular structure is essential for optimizing the desired properties of the final product. By harnessing the synthetic potential of this compound, chemists can access a wide array of chemical transformations, facilitating the creation of new molecules with enhanced biological activities or improved performance characteristics.