1. Home
  2. 2-Thiazolamine, 4-methyl-5-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-5-phenyl-

Nc1nc(c(s1)c1ccccc1)C Request for Quotation
Chemical Name: 2-Thiazolamine, 4-methyl-5-phenyl-
CAS Number: 28241-62-5
Product Number: AG00BGFB(AGN-PC-0JOHQ9)
Synonyms:
MDL No:
Molecular Formula: C10H10N2S
Molecular Weight: 190.2648

Identification/Properties

Properties
BP:
349.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
190.264g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
190.056g/mol
Monoisotopic Mass:
190.056g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
168
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

Request for Quotation

Customer Feedback

Chemical Structure


4-Methyl-5-phenylthiazol-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the construction of various complex molecules. Its aromatic phenyl ring and thiazole moiety make it an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, the presence of the amino group allows for further functionalization through various chemical reactions, such as acylation, alkylation, and halogenation. Overall, the application of 4-Methyl-5-phenylthiazol-2-amine in chemical synthesis showcases its significance as a key component in the creation of diverse compounds across different industries.