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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)-

SAFit1

CC(C=C1CC)=CC(CC)=C1C2=C(OC(C(C)(C([2H])([2H])[2H])C)=O)N3N(C2=O)CCOCC3 Request for Quotation
Chemical Name: SAFit1
CAS Number: 1643125-32-9
Product Number: AG01V5E0()
Synonyms:
MDL No:
Molecular Formula:
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Chemical Structure


SAFit1 is a versatile and innovative chemical reagent that plays a crucial role in enhancing the efficiency and selectivity of various chemical synthesis processes. This unique compound serves as a highly effective catalyst, facilitating a wide range of organic transformations with remarkable precision and speed. By leveraging the catalytic properties of SAFit1, chemists are able to streamline complex synthetic pathways, leading to accelerated reaction rates and improved product yields. Additionally, SAFit1 exhibits excellent compatibility with a diverse array of functional groups, making it a valuable tool for synthesizing intricate molecular structures with intricate regioselectivity and stereoselectivity. Whether used in pharmaceutical manufacturing, material science, or other research endeavors, SAFit1 stands as an indispensable asset for advancing the frontiers of chemical synthesis.