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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-Thiazolamine, 4,5-dimethyl-

Nc1sc(c(n1)C)C Request for Quotation
Chemical Name: 2-Thiazolamine, 4,5-dimethyl-
CAS Number: 2289-75-0
Product Number: AG002LDB(AGN-PC-0JLB01)
Synonyms:
MDL No:
Molecular Formula: C5H8N2S
Molecular Weight: 128.1954

Identification/Properties

Computed Properties
Molecular Weight:
128.193g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
128.041g/mol
Monoisotopic Mass:
128.041g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
86.5
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


4,5-Dimethylthiazol-2-amine, also known as MTT, is a versatile compound widely used in chemical synthesis. Its primary application lies in the field of biochemistry and molecular biology, where it serves as a colorimetric indicator for cell viability and proliferation assays. MTT is commonly employed in assessing cell metabolic activity by measuring the conversion of the yellow MTT reagent to a purple formazan product. This reaction provides a quantitative measure of cell viability and can be utilized in various research settings, including drug screening, toxicity studies, and cell culture optimization. Additionally, 4,5-Dimethylthiazol-2-amine can be utilized in the synthesis of various organic compounds, pharmaceuticals, and other chemical products, showcasing its importance across different industries. Its unique properties and diverse applications make it a valuable tool in scientific research and chemical synthesis methodologies.