1. Home
  2. Sulfamoyl chloride, ethylmethyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Sulfamoyl chloride, ethylmethyl-

CCN(S(=O)(=O)Cl)C Request for Quotation
Chemical Name: Sulfamoyl chloride, ethylmethyl-
CAS Number: 35856-61-2
Product Number: AG00D2J1(AGN-PC-03SWFK)
Synonyms:
MDL No:
Molecular Formula: C3H8ClNO2S
Molecular Weight: 157.6191

Identification/Properties

Computed Properties
Molecular Weight:
157.612g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
156.996g/mol
Monoisotopic Mass:
156.996g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
147
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3265
Hazard Statements:
H302-H312-H314-H332
Precautionary Statements:
P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl(methyl)sulfamoyl chloride, also known as N-ethoxycarbonylmethyl-N-methylsulfamoyl chloride, serves as a versatile reagent in chemical synthesis due to its unique functional groups and reactivity. This compound is commonly utilized as an acylating agent in organic reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. Its ability to introduce both ethyl and methyl groups to target molecules makes it a valuable building block in the creation of complex organic compounds. Additionally, ethyl(methyl)sulfamoyl chloride can participate in nucleophilic substitution reactions, allowing for the installation of sulfamoyl groups onto various substrates. Its role in chemical synthesis extends to the production of intermediates for dyes, polymers, and other specialty chemicals, making it a crucial component in the toolbox of synthetic chemists.