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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)-

CH3SO3H

CS(=O)(=O)O.CS(=O)(=O)O.CN(c1ccc2c(c1)Sc1c(N2)ccc(c1)N(C)C)C Request for Quotation
Chemical Name: CH3SO3H
CAS Number: 1236208-20-0
Product Number: AG009CN2(AGN-009CHI)
Synonyms:
MDL No:
Molecular Formula: C18H27N3O6S3
Molecular Weight: 477.6185

Identification/Properties

Computed Properties
Molecular Weight:
477.609g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
2
Exact Mass:
477.106g/mol
Monoisotopic Mass:
477.106g/mol
Topological Polar Surface Area:
169A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
396
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N3,N3,N7,N7-Tetramethyl-10H-phenothiazine-3,7-diamine dimethanesulfonate is a versatile compound widely utilized in chemical synthesis as a powerful catalyst in various reactions. Its unique structure and properties make it particularly effective in promoting organic transformations, such as aromatic substitutions, oxidation reactions, and cross-coupling reactions. This compound's high stability and reactivity under different reaction conditions make it a valuable tool in the development of new synthetic methodologies and the production of complex molecules with high efficiency.