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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)-

1-(4-chlorophenyl)cyclopropan-1-amine;hydrochloride

NC1(CC1)c1ccc(cc1)Cl.Cl Request for Quotation
Chemical Name: 1-(4-chlorophenyl)cyclopropan-1-amine;hydrochloride
CAS Number: 1009102-44-6
Product Number: AG00035R(AGN-PC-04H65Q)
Synonyms:
MDL No: MFCD07995727
Molecular Formula: C9H11Cl2N
Molecular Weight: 204.0963

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
204.094g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
203.027g/mol
Monoisotopic Mass:
203.027g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
146
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:
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


The 1-(4-Chlorophenyl)cyclopropanamine hydrochloride is a versatile compound commonly used in chemical synthesis as a building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique cyclopropane ring structure and the presence of a chlorophenyl group, this compound offers opportunities for the development of novel molecules with desirable properties.In chemical synthesis, 1-(4-Chlorophenyl)cyclopropanamine hydrochloride can serve as a key intermediate in the preparation of diverse compounds through structural modifications such as functional group transformations, ring-opening reactions, and substitution reactions. Its cyclopropane ring provides rigidity and steric effects that can influence the reactivity and selectivity of reactions, making it a valuable starting material for the synthesis of complex molecules.Furthermore, the presence of the chlorophenyl group in 1-(4-Chlorophenyl)cyclopropanamine hydrochloride enables the introduction of additional functional groups through various chemical reactions, allowing for the synthesis of structurally diverse compounds with potential biological activities or other desired properties.Overall, the application of 1-(4-Chlorophenyl)cyclopropanamine hydrochloride in chemical synthesis offers researchers and chemists a valuable tool for the efficient and strategic construction of novel molecules with potential applications in the fields of medicine, agriculture, and materials science.