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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)-

2-(2-methoxyethoxy)ethane-1-sulfonyl chloride

COCCOCCS(=O)(=O)Cl Request for Quotation
Chemical Name: 2-(2-methoxyethoxy)ethane-1-sulfonyl chloride
CAS Number: 1215974-61-0
Product Number: AG00VTXA(AGN-PC-0WBKM4)
Synonyms:
MDL No: MFCD14529336
Molecular Formula: C5H11ClO4S
Molecular Weight: 202.6564

Identification/Properties

Computed Properties
Molecular Weight:
202.649g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
202.007g/mol
Monoisotopic Mass:
202.007g/mol
Topological Polar Surface Area:
61A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
171
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


2-(2-Methoxyethoxy)ethane-1-sulfonyl chloride, also known as Methyl-2-(2-chloroethoxy)ethyl sulfone, is a versatile compound widely used in chemical synthesis as a sulfonyl chloride derivative. This compound is particularly valued for its ability to serve as a sulfonating agent in organic reactions. Its reactivity and unique chemical properties make it a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, 2-(2-Methoxyethoxy)ethane-1-sulfonyl chloride is frequently employed as a key intermediate in the functionalization of organic molecules, where it enables the introduction of sulfonyl groups into target compounds. Its applications extend to the synthesis of sulfonamides, sulfonylureas, and sulfonate esters, among others. Furthermore, the sulfonyl chloride functionality of this compound allows for efficient and selective derivatization of alcohols, amines, and other nucleophilic groups, making it a valuable tool in the creation of complex molecular architectures. Additionally, 2-(2-Methoxyethoxy)ethane-1-sulfonyl chloride finds utility as a protecting group in organic synthesis, safeguarding specific functional groups during chemical transformations and facilitating selective reactions. This compound's broad range of applications underscores its importance in modern chemical synthesis as a versatile and indispensable reagent.