1. Home
  2. Sulfamide, propyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Sulfamide, propyl-

CCCNS(=O)(=O)N Request for Quotation
Chemical Name: Sulfamide, propyl-
CAS Number: 147962-41-2
Product Number: AG001FC2(AGN-PC-00OGE0)
Synonyms:
MDL No:
Molecular Formula: C3H10N2O2S
Molecular Weight: 138.1887

Identification/Properties

Computed Properties
Molecular Weight:
138.185g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
138.046g/mol
Monoisotopic Mass:
138.046g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
134
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

Request for Quotation

Customer Feedback

Chemical Structure


N-Propylsulfamide is a versatile compound that finds valuable applications in chemical synthesis. This compound is commonly used as a reagent in organic reactions, where it serves as a sulfonamide source. N-Propylsulfamide can be used to introduce the sulfonamide functional group into various organic molecules, allowing for the synthesis of new and complex chemical substances. Additionally, this compound can act as a nucleophile in reactions with electrophiles, facilitating the formation of new carbon-nitrogen bonds. With its ability to participate in a range of reactions, N-Propylsulfamide is an important tool for chemists working in the field of organic synthesis.