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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)-

1-Naphthalenesulfonamide, N-(6-aminohexyl)-, monohydrochloride

NCCCCCCNS(=O)(=O)c1cccc2c1cccc2.Cl Request for Quotation
Chemical Name: 1-Naphthalenesulfonamide, N-(6-aminohexyl)-, monohydrochloride
CAS Number: 61714-25-8
Product Number: AG003SDR(AGN-PC-0T1F97)
Synonyms:
MDL No:
Molecular Formula: C16H23ClN2O2S
Molecular Weight: 342.8840

Identification/Properties

Properties
MP:
161-163ºC
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
342.882g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
342.117g/mol
Monoisotopic Mass:
342.117g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
392
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


W-5 HCl, also known as hydrochloric acid with a concentration of 5%, plays a vital role in chemical synthesis processes. This solution of hydrochloric acid is widely utilized as a catalyst and reagent in various reactions due to its moderate strength and versatility. In organic chemistry, W-5 HCl can be employed for the activation of carbonyl compounds, such as acid chlorides and anhydrides, facilitating nucleophilic substitution reactions. Additionally, it is commonly employed in the hydrolysis of esters to yield carboxylic acids, an essential transformation in the production of pharmaceuticals, polymers, and other organic compounds. In inorganic synthesis, W-5 HCl is utilized for the dissolution of metal oxides and insoluble metal salts to generate soluble metal chlorides, enabling subsequent purification and isolation processes. Moreover, in the field of materials chemistry, it serves as a crucial etchant for metals and semiconductors, enabling precise patterning and structuring of surfaces. Overall, W-5 HCl is a fundamental and versatile reagent in chemical synthesis, facilitating a wide range of transformations and reactions across various disciplines.