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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-methyl-N-phenyl-

Cc1csc(n1)Nc1ccccc1 Request for Quotation
Chemical Name: 2-Thiazolamine, 4-methyl-N-phenyl-
CAS Number: 90916-46-4
Product Number: AG00GUF9(AGN-PC-0JUSTF)
Synonyms:
MDL No:
Molecular Formula: C10H10N2S
Molecular Weight: 190.2648

Identification/Properties

Properties
BP:
316.2 °C at 760 mmHg
Computed Properties
Molecular Weight:
190.264g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
190.056g/mol
Monoisotopic Mass:
190.056g/mol
Topological Polar Surface Area:
53.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
157
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


4-Methyl-N-phenyl-2-thiazolamine, a chemical compound with a unique molecular structure, plays a crucial role in chemical synthesis processes. This versatile compound is widely utilized in organic chemistry as a key building block for the synthesis of various complex molecules and pharmaceutical intermediates. With its distinctive thiazole ring and functional groups, 4-Methyl-N-phenyl-2-thiazolamine serves as a valuable starting material in the preparation of novel heterocyclic compounds. Its presence in chemical reactions can lead to the formation of diverse products with enhanced properties and potential applications in drug discovery, material science, and agrochemical development. Additionally, the reactivity and stability of this compound make it an important tool for organic chemists seeking to engage in innovative synthetic strategies and explore new avenues in molecular design.