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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-(1,3-thiazol-2-yl)ethanamine;hydrochloride

CC(c1nccs1)N.Cl Request for Quotation
Chemical Name: 1-(1,3-thiazol-2-yl)ethanamine;hydrochloride
CAS Number: 947662-64-8
Product Number: AG003CVQ(AGN-PC-0BGIFU)
Synonyms:
MDL No: MFCD11846195
Molecular Formula: C5H9ClN2S
Molecular Weight: 164.6564

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
164.66g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
164.017497g/mol
Monoisotopic Mass:
164.017497g/mol
Topological Polar Surface Area:
67.2Ų
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
76.8
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:
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 compound 1-(Thiazol-2-yl)ethanamine hydrochloride, also known as $name$, is a versatile chemical reagent commonly used in chemical synthesis processes. This compound serves as a key building block in the creation of various organic molecules due to its unique structure and reactivity.In chemical synthesis, 1-(Thiazol-2-yl)ethanamine hydrochloride is frequently employed as a nucleophilic reactant in the formation of more complex compounds. Its thiazole ring imparts aromatic and heterocyclic properties, allowing for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the ethanamine moiety provides a primary amine functionality, which can participate in a range of reactions such as acylation, alkylation, and condensation.Furthermore, the hydrochloride salt form of this compound enhances its solubility in aqueous environments, making it particularly useful in reactions that require both organic and aqueous phases. Its high purity and stability ensure consistent performance in various synthetic protocols.Overall, the application of 1-(Thiazol-2-yl)ethanamine hydrochloride in chemical synthesis enables the efficient and reliable construction of diverse molecules with pharmaceutical, agricultural, and industrial significance.