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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)-

Thiazole,2-hydrazinyl-4,5-dimethyl-

NNc1sc(c(n1)C)C Request for Quotation
Chemical Name: Thiazole,2-hydrazinyl-4,5-dimethyl-
CAS Number: 124285-37-6
Product Number: AG000LT5(AGN-PC-0PHS85)
Synonyms:
MDL No:
Molecular Formula: C5H9N3S
Molecular Weight: 143.2101

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Hydrazinyl-4,5-dimethylthiazole is a versatile compound widely utilized in chemical synthesis as a valuable building block. Due to its unique structure and reactivity, it serves as a key intermediate in the preparation of various functionalized molecules with diverse applications.In organic synthesis, 2-Hydrazinyl-4,5-dimethylthiazole acts as a nucleophilic reagent, participating in reactions such as nucleophilic substitution, condensation, and cyclization. Its hydrazine group is highly reactive towards electrophiles, enabling the formation of new carbon-nitrogen bonds and facilitating the synthesis of heterocyclic compounds.Furthermore, the presence of the thiazole ring in 2-Hydrazinyl-4,5-dimethylthiazole imparts aromaticity and stability to the molecule, making it a suitable component for the construction of pharmaceutical intermediates, agrochemicals, and materials with desired properties. Its ability to undergo various transformations under mild reaction conditions makes it a valuable tool in the hands of synthetic chemists for the creation of complex molecules with specific functionalities and applications.