1. Home
  2. (4-phenyl-1,3-thiazol-2-yl)hydrazine

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)-

(4-phenyl-1,3-thiazol-2-yl)hydrazine

NNc1scc(n1)c1ccccc1 Request for Quotation
Chemical Name: (4-phenyl-1,3-thiazol-2-yl)hydrazine
CAS Number: 34176-52-8
Product Number: AG00C7BK(AGN-PC-0JM33X)
Synonyms:
MDL No:
Molecular Formula: C9H9N3S
Molecular Weight: 191.2529

Identification/Properties

Computed Properties
Molecular Weight:
191.252g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
191.052g/mol
Monoisotopic Mass:
191.052g/mol
Topological Polar Surface Area:
79.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
159
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:
Danger
UN#:
2811
Hazard Statements:
H301-H318
Precautionary Statements:
P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Hydrazinyl-4-phenylthiazole, a versatile compound utilized in chemical synthesis, plays a crucial role in various reactions due to its unique properties. This compound is commonly employed as a key intermediate in the preparation of pharmaceuticals, pesticides, and other organic compounds. Its hydrazine functional group allows for the formation of important derivatives through a variety of reactions, including condensation, reduction, and oxidation. Furthermore, the thiazole ring in 2-Hydrazinyl-4-phenylthiazole provides additional opportunities for structural modification, enabling the synthesis of diverse compounds with potentially valuable biological activities. This compound stands out as a valuable building block in the realm of chemical synthesis, offering chemists a versatile tool for the creation of novel compounds with potential applications in various fields of chemistry.