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  2. 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzamide

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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)-

2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzamide

CC(=CCSc1ccccc1C(=O)N)CC/C=C(/CCC=C(C)C)C Request for Quotation
Chemical Name: 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzamide
CAS Number: 1092521-74-8
Product Number: AG007TE1(AGN-PC-04XJD7)
Synonyms:
MDL No: MFCD11976913
Molecular Formula: C22H31NOS
Molecular Weight: 357.5526

Identification/Properties

Computed Properties
Molecular Weight:
357.556g/mol
XLogP3:
6.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
10
Exact Mass:
357.213g/mol
Monoisotopic Mass:
357.213g/mol
Topological Polar Surface Area:
68.4A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
500
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Farnesyl Thiosalicylic Acid Amide is a versatile compound that finds significant application in chemical synthesis. With its unique structure and reactive properties, this compound is commonly used as a key intermediate in the synthesis of various bioactive molecules and pharmaceuticals.Due to its ability to undergo selective chemical reactions and form important bonds, Farnesyl Thiosalicylic Acid Amide serves as a valuable building block in organic synthesis. Its sulfur-containing functional group enables diverse transformations, making it ideal for introducing structural complexity into target molecules.In addition, Farnesyl Thiosalicylic Acid Amide is often utilized in the development of novel drug candidates and pharmaceutical intermediates. By incorporating this compound into synthetic pathways, chemists can access a wide range of derivatives with potential therapeutic benefits.Furthermore, the reactivity and stability of Farnesyl Thiosalicylic Acid Amide make it a preferred choice for creating molecular scaffolds with specific functionalities. Its compatibility with various reaction conditions and protocols allows for efficient and reliable synthesis of complex molecules with tailored properties.Overall, Farnesyl Thiosalicylic Acid Amide plays a crucial role in advancing chemical synthesis strategies, enabling the construction of diverse molecular architectures and facilitating the discovery of new compounds with potential applications in medicine, agrochemicals, and materials science.