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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)-

4-[2-(bromomethyl)phenyl]sulfonylmorpholine

BrCc1ccccc1S(=O)(=O)N1CCOCC1 Request for Quotation
Chemical Name: 4-[2-(bromomethyl)phenyl]sulfonylmorpholine
CAS Number: 941717-06-2
Product Number: AG006PAF(AGN-PC-04G0RU)
Synonyms:
MDL No:
Molecular Formula: C11H14BrNO3S
Molecular Weight: 320.2028

Identification/Properties

Properties
MP:
71.5-73.5℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
320.201g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
318.988g/mol
Monoisotopic Mass:
318.988g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
335
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:
Warning
UN#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-((2-(Bromomethyl)phenyl)sulfonyl)morpholine, also known as $name$, is a versatile compound used in chemical synthesis for various applications. In organic chemistry, this molecule serves as a valuable building block for the creation of complex structures due to its unique reactivity and functional groups.One of the key applications of $name$ in chemical synthesis is its role as a sulfonylating agent. The presence of the sulfonyl group provides an opportunity for selective functionalization of organic molecules, allowing chemists to introduce specific chemical moieties at desired positions. This makes $name$ a valuable tool for the modification of organic compounds in a controlled and predictable manner.Furthermore, $name$ can also act as a nucleophilic sulfonating agent, facilitating the formation of sulfonamide derivatives. By reacting with various nucleophiles, such as amines or alcohols, $name$ enables the synthesis of diverse sulfonamide-containing compounds with potential biological activities or industrial applications.Additionally, the morpholine ring in $name$ confers unique steric and electronic properties that can influence the reactivity and selectivity of chemical reactions. This makes $name$ a versatile reagent for the construction of heterocyclic compounds and pharmaceutical intermediates, opening up possibilities for the development of new drugs or materials.Overall, the application of 4-((2-(Bromomethyl)phenyl)sulfonyl)morpholine in chemical synthesis offers a toolbox of synthetic strategies for the creation of complex molecules with tailored properties and functionalities.