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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-(3-chlorophenyl)propan-1-amine

CCC(c1cccc(c1)Cl)N Request for Quotation
Chemical Name: 1-(3-chlorophenyl)propan-1-amine
CAS Number: 40023-86-7
Product Number: AG00CITF(AGN-PC-013P03)
Synonyms:
MDL No:
Molecular Formula: C9H12ClN
Molecular Weight: 169.6513

Identification/Properties

Computed Properties
Molecular Weight:
169.652g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
169.066g/mol
Monoisotopic Mass:
169.066g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
116
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-α-ethylbenzenemethanamine, also known as $name$, is a versatile compound commonly utilized in chemical synthesis for various applications. In particular, this compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One of the notable applications of 3-Chloro-α-ethylbenzenemethanamine in chemical synthesis is its role as an intermediate in the production of organic compounds with biological activity. By strategically incorporating this compound into multi-step synthesis routes, chemists can efficiently access structurally complex molecules that exhibit potential therapeutic or agricultural effects.Moreover, due to the unique structural features of 3-Chloro-α-ethylbenzenemethanamine, it can participate in a range of chemical reactions, such as nucleophilic substitution, reductive amination, and palladium-catalyzed coupling reactions. These diverse reactivity profiles make this compound a valuable tool for chemists seeking to construct intricate molecular architectures with tailored properties.Overall, the strategic incorporation of 3-Chloro-α-ethylbenzenemethanamine in chemical synthesis enables researchers to access novel compounds with biological relevance and fine-tuned functionalities, highlighting its importance in the field of organic chemistry.