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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)-

Benzo[b]thiophene-3-carboxamide,2-[(3,4-dimethoxybenzoyl)amino]-4,5,6,7-tetrahydro-

COc1cc(ccc1OC)C(=O)Nc1sc2c(c1C(=O)N)CCCC2 Request for Quotation
Chemical Name: Benzo[b]thiophene-3-carboxamide,2-[(3,4-dimethoxybenzoyl)amino]-4,5,6,7-tetrahydro-
CAS Number: 301305-73-7
Product Number: AG003UHX(AGN-PC-0R5IHS)
Synonyms:
MDL No:
Molecular Formula: C18H20N2O4S
Molecular Weight: 360.4274

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Stability:
Light Sensitive
Solubility:
H2O:
Computed Properties
Molecular Weight:
360.428g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
360.114g/mol
Monoisotopic Mass:
360.114g/mol
Topological Polar Surface Area:
119A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
504
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


TCS 359 is a versatile and highly effective catalyst commonly used in chemical synthesis processes. This catalyst plays a crucial role in promoting various reactions by facilitating the conversion of reactants into desired products with high selectivity and efficiency. Its unique properties make it particularly useful in a wide range of applications within the field of organic chemistry.One key application of TCS 359 in chemical synthesis is in the field of asymmetric catalysis. As an asymmetric catalyst, TCS 359 has the ability to induce chirality in a molecule, resulting in the formation of optically active compounds. This is especially important in the pharmaceutical and agrochemical industries, where enantiopure compounds are essential for the development of new drugs and other biologically active molecules.Additionally, TCS 359 is commonly utilized in cross-coupling reactions, a fundamental tool in organic synthesis for forming carbon-carbon and carbon-heteroatom bonds. The catalyst's high efficiency and selectivity enable the precise control of reaction conditions, leading to the desired bond formations with minimal byproducts. This is especially valuable in the production of complex molecules and natural products.Furthermore, TCS 359 is known for its stability and compatibility with a wide range of functional groups, making it a versatile and reliable choice for synthetic chemists. Whether in academic research settings or industrial production processes, the application of TCS 359 in chemical synthesis has proven instrumental in advancing the field of organic chemistry and enabling the efficient preparation of valuable compounds.