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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)-

Octane, 1,8-diisothiocyanato-

S=C=NCCCCCCCCN=C=S Request for Quotation
Chemical Name: Octane, 1,8-diisothiocyanato-
CAS Number: 56312-14-2
Product Number: AG00EB9E(AGN-PC-0JMT7B)
Synonyms:
MDL No:
Molecular Formula: C10H16N2S2
Molecular Weight: 228.37744

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Chemical Structure


$Name$ is a powerful chemical reagent used in various chemical synthesis processes. With its unique properties, it is commonly employed in the production of specialty chemicals, pharmaceutical intermediates, and polymer materials. This versatile compound plays a crucial role in organic synthesis, particularly in the formation of complex organic molecules. Its ability to react readily with a wide range of functional groups makes it highly desired in research and development settings. Additionally, 1,8-Octane Diisothiocyanate exhibits excellent compatibility with various solvents and reaction conditions, making it a valuable tool for synthetic chemists seeking to access novel compounds efficiently and effectively. Utilizing $Name$ in chemical synthesis not only enables the synthesis of intricate molecular structures but also offers opportunities for exploring new reactions and pathways in the field of organic chemistry.