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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)-

2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride

Clc1ccc(c(c1)Cl)C(N)(C)C.Cl Request for Quotation
Chemical Name: 2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride
CAS Number: 1216497-60-7
Product Number: AG0015HQ(AGN-PC-0WANHI)
Synonyms:
MDL No:
Molecular Formula: C9H12Cl3N
Molecular Weight: 240.5573

Identification/Properties

Computed Properties
Molecular Weight:
240.552g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
239.004g/mol
Monoisotopic Mass:
239.004g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
159
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride is a versatile compound widely utilized in chemical synthesis due to its unique properties. This compound, also known as $name$, serves as a valuable building block in the creation of various organic molecules through its involvement in multiple chemical reactions.In chemical synthesis, the application of 2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride is crucial for the formation of complex structures in pharmaceuticals, agrochemicals, and materials science. This compound acts as a key intermediate in the synthesis of diverse compounds, enabling the modification and enhancement of specific functional groups within the target molecules.Furthermore, 2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride plays a significant role in the development of novel organic compounds with specialized properties, such as bioactive substances, fluorescent dyes, and advanced materials. Its reactivity and compatibility with various catalysts make it a valuable tool for chemists seeking to create innovative chemical structures for a wide range of applications.Overall, the application of 2-(2,4-Dichlorophenyl)propan-2-amine hydrochloride in chemical synthesis offers a realm of possibilities for researchers and industry professionals alike, driving advancements in diverse fields of chemistry and material science.