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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)-

Ethanamine, 2-[(phenylmethyl)thio]-, hydrochloride

NCCSCc1ccccc1.Cl Request for Quotation
Chemical Name: Ethanamine, 2-[(phenylmethyl)thio]-, hydrochloride
CAS Number: 22572-33-4
Product Number: AG003U7F(AGN-PC-00L8ZI)
Synonyms:
MDL No:
Molecular Formula: C9H14ClNS
Molecular Weight: 203.7322

Identification/Properties

Computed Properties
Molecular Weight:
203.728g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
203.054g/mol
Monoisotopic Mass:
203.054g/mol
Topological Polar Surface Area:
51.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
89.6
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Benzylthio)ethanamine hydrochloride is a versatile compound that finds widespread utility in chemical synthesis, particularly in organic chemistry reactions. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the prominent applications of 2-(Benzylthio)ethanamine hydrochloride is in the synthesis of complex organic molecules such as amino acids, peptides, and heterocyclic compounds. Its ability to undergo nucleophilic substitution reactions makes it a valuable building block in the creation of diverse chemical entities.Furthermore, this compound plays a crucial role in the modification of natural products and the development of novel drug candidates. Its functional group reactivity enables the selective introduction of specific chemical functionalities, leading to the generation of structurally diverse compounds with potential biological activities.In summary, the application of 2-(Benzylthio)ethanamine hydrochloride in chemical synthesis encompasses its use as a key intermediate for the production of pharmaceuticals, agrochemicals, and specialty chemicals, as well as its role in the synthesis of complex organic molecules and drug discovery efforts.