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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)-

Cyclopropanamine, 2-phenyl-, (1R,2S)-rel-, sulfate (2:1)

OS(=O)(=O)O.N[C@@H]1C[C@H]1c1ccccc1.N[C@@H]1C[C@H]1c1ccccc1 Request for Quotation
Chemical Name: Cyclopropanamine, 2-phenyl-, (1R,2S)-rel-, sulfate (2:1)
CAS Number: 13492-01-8
Product Number: AG009AI7(AGN-PC-0PKFZ4)
Synonyms:
MDL No:
Molecular Formula: C18H24N2O4S
Molecular Weight: 364.4592

Identification/Properties

Computed Properties
Molecular Weight:
364.46g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
364.146g/mol
Monoisotopic Mass:
364.146g/mol
Topological Polar Surface Area:
135A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
197
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H300-H311+H331
Precautionary Statements:
P261-P280-P302+P352+P312-P304+P340+P312-P403+P233
Class:
6.1
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The trans-2-Phenylcyclopropylamine hemisulfate salt is a versatile chemical compound commonly utilized in chemical synthesis due to its unique structural properties. This compound serves as a valuable building block in the creation of various molecules, offering opportunities for selective transformations and novel product development. Its use in organic synthesis enables the development of complex molecules with specific stereochemistry, making it a valuable tool for researchers and chemists alike. By incorporating trans-2-Phenylcyclopropylamine hemisulfate salt into chemical reactions, precise control over the stereochemical outcome can be achieved, leading to the synthesis of diverse and interesting compounds. This compound's applications extend across a range of research fields, including medicinal chemistry, materials science, and drug discovery, highlighting its significance in advancing scientific endeavors.