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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)-

Phenol, 4-[(5,6-dihydro-4H-1,3-thiazin-2-yl)amino]-3,5-dimethyl-

Oc1cc(C)c(c(c1)C)NC1=NCCCS1 Request for Quotation
Chemical Name: Phenol, 4-[(5,6-dihydro-4H-1,3-thiazin-2-yl)amino]-3,5-dimethyl-
CAS Number: 145356-32-7
Product Number: AG001KUI(AGN-PC-07Y4NS)
Synonyms:
MDL No:
Molecular Formula: C12H16N2OS
Molecular Weight: 236.3332

Identification/Properties

Computed Properties
Molecular Weight:
236.333g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
236.098g/mol
Monoisotopic Mass:
236.098g/mol
Topological Polar Surface Area:
69.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
258
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(5,6-Dihydro-4H-1,3-thiazin-2-ylamino)-3,5-dimethyl-phenol, also known as $name$, is a versatile compound commonly used in chemical synthesis. Its unique structure makes it a valuable tool in various chemical reactions and reactions. One prominent application of $name$ in chemical synthesis is as a reagent in the preparation of novel heterocyclic compounds. By leveraging the thiazine ring and phenol group present in its structure, chemists can efficiently introduce these moieties into target molecules, allowing for the synthesis of diverse compounds with potential pharmaceutical or materials science applications.Additionally, the amino group attached to the thiazine ring in $name$ can serve as a nucleophilic site in various synthetic transformations, enabling selective functionalization of molecules in complex synthesis routes. This reactivity profile makes $name$ a valuable building block for designing and constructing structurally intricate molecules in organic chemistry.Overall, the application of 4-(5,6-Dihydro-4H-1,3-thiazin-2-ylamino)-3,5-dimethyl-phenol in chemical synthesis highlights its significance as a versatile intermediate in the creation of novel compounds with tailored properties and functionalities.