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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)-

Methyl-(2-phenyl-thiazol-4-ylmethyl)-amine / N-methyl-1-(2-phenyl-1,3-thiazol-4-yl)methanamine

CNCc1csc(n1)c1ccccc1 Request for Quotation
Chemical Name: Methyl-(2-phenyl-thiazol-4-ylmethyl)-amine / N-methyl-1-(2-phenyl-1,3-thiazol-4-yl)methanamine
CAS Number: 921101-66-8
Product Number: AG00H55E(AGN-PC-0WAL4E)
Synonyms:
MDL No:
Molecular Formula: C11H12N2S
Molecular Weight: 204.2914

Identification/Properties

Computed Properties
Molecular Weight:
204.291g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
204.072g/mol
Monoisotopic Mass:
204.072g/mol
Topological Polar Surface Area:
53.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
169
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


N-Methyl-1-(2-phenylthiazol-4-yl)methanamine is a versatile compound that finds wide applications in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various organic molecules. In organic chemistry, this compound is commonly used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds. Its ability to undergo different types of reactions, such as substitution, condensation, and addition reactions, allows for the creation of diverse chemical structures. Chemists often utilize N-Methyl-1-(2-phenylthiazol-4-yl)methanamine as a starting material to introduce specific functional groups or stereochemistry into target molecules, enabling the synthesis of new compounds with tailored properties and potential applications.