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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)propyl]amine dihydrochloride

CCC(c1nccs1)N.Cl.Cl Request for Quotation
Chemical Name: [1-(1,3-thiazol-2-yl)propyl]amine dihydrochloride
CAS Number: 1255717-87-3
Product Number: AG00J16K(AG00J16K)
Synonyms:
MDL No:
Molecular Formula: C6H12Cl2N2S
Molecular Weight: 215.1439

Identification/Properties

Computed Properties
Molecular Weight:
215.136g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
214.01g/mol
Monoisotopic Mass:
214.01g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
87.1
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Thiazolemethanamine, α-ethyl-, hydrochloride (1:2) is a key reagent utilized in chemical synthesis for its valuable properties in various reactions. This compound is commonly employed as a versatile building block in the creation of pharmaceutical intermediates, agrochemicals, and other fine chemicals. Its role in chemical synthesis extends to the formation of heterocyclic compounds and derivatives with pharmaceutical significance. Additionally, 2-Thiazolemethanamine, α-ethyl-, hydrochloride (1:2) serves as a valuable precursor in the synthesis of complex organic molecules through various functional group transformations and synthetic pathways. Its presence in the laboratory enables chemists to access diverse chemical structures that are pivotal in drug discovery and material science research.