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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)-

SAG

CN[C@@H]1CC[C@H](CC1)N(C(=O)c1sc2c(c1Cl)cccc2)Cc1cccc(c1)c1ccncc1 Request for Quotation
Chemical Name: SAG
CAS Number: 912545-86-9
Product Number: AG003AA8(AGN-PC-0WAL5Z)
Synonyms:
MDL No:
Molecular Formula: C28H28ClN3OS
Molecular Weight: 490.0594

Identification/Properties

Computed Properties
Molecular Weight:
490.062g/mol
XLogP3:
6.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
489.164g/mol
Monoisotopic Mass:
489.164g/mol
Topological Polar Surface Area:
73.5A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
666
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
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


3-Chloro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]benzo[b]thiophene-2-carboxamide is a versatile compound widely utilized in the field of chemical synthesis. This compound serves as a valuable building block in the development of novel pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, this compound acts as a key intermediate in the preparation of various biologically active molecules. Its functional groups allow for facile modification and derivatization, enabling chemists to introduce specific functionalities or structural motifs required for enhancing the desired biological activity or properties of the final compound.One of the primary applications of 3-Chloro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]benzo[b]thiophene-2-carboxamide in chemical synthesis is in the development of novel pharmaceutical agents. By leveraging its unique molecular scaffold, chemists can explore different synthetic strategies to create potential drug candidates with enhanced efficacy, reduced side effects, and improved pharmacokinetic properties.Furthermore, this compound plays a crucial role in the synthesis of specialized organic molecules used in materials science and agrochemical research. Its presence in the molecular structure of these compounds imparts specific properties or functionalities, making them ideal for applications in various industries.Overall, 3-Chloro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]benzo[b]thiophene-2-carboxamide is a valuable tool for chemists engaged in the design and synthesis of diverse chemical entities with potential applications in pharmaceuticals, agrochemicals, and materials science.