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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)-

Acetamide, N,N'-[iminobis(sulfonyl-1,3,4-thiadiazole-5,2-diyl)]bis-

CC(=O)Nc1nnc(s1)S(=O)(=O)NS(=O)(=O)c1nnc(s1)NC(=O)C Request for Quotation
Chemical Name: Acetamide, N,N'-[iminobis(sulfonyl-1,3,4-thiadiazole-5,2-diyl)]bis-
CAS Number: 80495-47-2
Product Number: AG00G4T2(AGN-PC-0OIEEQ)
Synonyms:
MDL No:
Molecular Formula: C8H9N7O6S4
Molecular Weight: 427.46036

Identification/Properties

Computed Properties
Molecular Weight:
427.443g/mol
XLogP3:
-1.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
13
Rotatable Bond Count:
6
Exact Mass:
426.95g/mol
Monoisotopic Mass:
426.95g/mol
Topological Polar Surface Area:
263A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
669
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


The application of Bis[5-(acetylamino)-1,3,4-thiadiazole-2-sulfonyl]amine in chemical synthesis lies in its versatile reactivity and functional group compatibility. As a key building block, this compound serves as a valuable intermediate in the synthesis of various organic molecules with pharmaceutical, agrochemical, and material science applications. Its unique structure containing both sulfonyl and N-acetylamino moieties allows for selective and efficient functionalization through a variety of chemical reactions, including acylation, sulfonation, and cross-coupling reactions. By incorporating this compound into synthetic routes, chemists can access a diverse array of complex molecules with tailored properties and functionalities, making it a valuable tool in modern organic synthesis strategies.