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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)-

1,2,3-Trithiane-4-pentanoic Acid

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Chemical Name: 1,2,3-Trithiane-4-pentanoic Acid
CAS Number: 1204245-29-3
Product Number: AG008WHC(AGN-PC-0WA41X)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


5-(1,2,3-Trithian-4-yl)pentanoic acid is a versatile compound widely used in chemical synthesis as a building block for various organic molecules. Its unique structure, incorporating a trithiane moiety, imparts specific reactivity and functionality that make it valuable in organic chemistry applications.One key application of 5-(1,2,3-Trithian-4-yl)pentanoic acid is in the synthesis of heterocyclic compounds. The trithiane group can serve as a masked thiol, allowing for selective deprotection under specific conditions to reveal reactive thiol functionality. This feature is particularly valuable in the construction of complex molecules where precise control over thiol reactivity is required.Furthermore, the presence of the pentanoic acid moiety provides a handle for further derivatization, enabling the introduction of various functional groups or modifications to tailor the compound for specific applications. This flexibility makes 5-(1,2,3-Trithian-4-yl)pentanoic acid a valuable tool for synthetic chemists seeking to access diverse chemical structures efficiently and selectively.