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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-(1,3-thiazol-2-yl)propan-2-amine

CC(c1nccs1)(N)C Request for Quotation
Chemical Name: 2-(1,3-thiazol-2-yl)propan-2-amine
CAS Number: 1082393-38-1
Product Number: AG019UP5(AGN-PC-05C6UG)
Synonyms:
MDL No:
Molecular Formula: C6H10N2S
Molecular Weight: 142.2220

Identification/Properties

Computed Properties
Molecular Weight:
142.22g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
142.056g/mol
Monoisotopic Mass:
142.056g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Thiazol-2-yl)propan-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of a variety of organic molecules due to its distinctive properties and reactivity. Its primary application lies in the formation of diverse pharmacologically active compounds, particularly in the development of potential drug candidates and pharmaceutical intermediates.
                                
One key area where 2-(Thiazol-2-yl)propan-2-amine finds utility is in the synthesis of heterocyclic compounds. By incorporating this amine into reaction pathways, chemists can access a range of complex molecules with enhanced biological activities. Moreover, its unique thiazole moiety imparts specific functionalities that can be further modified or elaborated to tailor the desired chemical properties of the final product.
                                
Furthermore, 2-(Thiazol-2-yl)propan-2-amine serves as a crucial intermediate in the preparation of various functional materials. Its presence in the synthesis of polymers, ligands, and other specialty chemicals contributes to the development of innovative materials with specific applications in diverse industries, such as pharmaceuticals, agrochemicals, and materials science.
                                
In conclusion, the strategic incorporation of 2-(Thiazol-2-yl)propan-2-amine into synthetic routes enables chemists to access a broad spectrum of structurally diverse compounds with significant biological and chemical relevance. Its role as a versatile building block underscores its importance in advancing the field of chemical synthesis and drug discovery.