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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-phenyl-, hydrochloride

NCC1(CC1)c1ccccc1.Cl Request for Quotation
Chemical Name: Cyclopropanemethanamine, 1-phenyl-, hydrochloride
CAS Number: 935-43-3
Product Number: AG003BFN(AGN-PC-03EVJT)
Synonyms:
MDL No:
Molecular Formula: C10H14ClN
Molecular Weight: 183.6779

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
183.679g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
183.081g/mol
Monoisotopic Mass:
183.081g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
132
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H319
Precautionary Statements:
P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1-Phenylcyclopropyl)methylamine Hydrochloride is a versatile molecule commonly used in chemical synthesis as a valuable building block for the preparation of various organic compounds. Its unique structure allows it to participate in a wide range of reactions, making it a valuable tool for synthetic chemists.In particular, (1-Phenylcyclopropyl)methylamine Hydrochloride serves as a key intermediate in the synthesis of complex organic molecules with pharmaceutical or agrochemical applications. Its presence in the reaction mixtures can facilitate the formation of important functional groups or assist in the creation of specific stereochemical configurations in the final products.Furthermore, the incorporation of (1-Phenylcyclopropyl)methylamine Hydrochloride into organic syntheses can enable the production of novel compounds with enhanced biological activities or improved pharmacokinetic properties. Its reactivity and compatibility with various reaction conditions make it a valuable reagent for the preparation of structurally diverse molecules with potential use in drug discovery and development.Overall, the application of (1-Phenylcyclopropyl)methylamine Hydrochloride in chemical synthesis showcases its utility as a valuable resource for accessing complex organic structures with tailored properties and functionalities.