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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-(4-methyl-1,3-thiazol-5-yl)ethanamine;hydrochloride

Cc1ncsc1CCN.Cl Request for Quotation
Chemical Name: 2-(4-methyl-1,3-thiazol-5-yl)ethanamine;hydrochloride
CAS Number: 17928-09-5
Product Number: AG0026WH(AGN-PC-0JN0LE)
Synonyms:
MDL No:
Molecular Formula: C6H11ClN2S
Molecular Weight: 178.6829

Identification/Properties

Computed Properties
Molecular Weight:
178.678g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
178.033g/mol
Monoisotopic Mass:
178.033g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
87.1
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


2-(4-Methylthiazol-5-yl)ethanamine hydrochloride is a versatile compound widely utilized in chemical synthesis for the preparation of various organic molecules. This compound serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for selective functionalization at the amino group, enabling the introduction of specific chemical moieties to tailor the properties of the final product. Additionally, 2-(4-Methylthiazol-5-yl)ethanamine hydrochloride can participate in diverse chemical reactions such as nucleophilic substitution, condensation, and cyclization, making it a valuable tool for organic chemists in designing and executing complex synthetic routes.