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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-Propenoic acid, 3-[3-(chlorosulfonyl)phenyl]-, methyl ester, (2E)-

COC(=O)/C=C/c1cccc(c1)S(=O)(=O)Cl Request for Quotation
Chemical Name: 2-Propenoic acid, 3-[3-(chlorosulfonyl)phenyl]-, methyl ester, (2E)-
CAS Number: 610801-83-7
Product Number: AG003RIR(AGN-PC-0OD9HO)
Synonyms:
MDL No: MFCD25973463
Molecular Formula: C10H9ClO4S
Molecular Weight: 260.6941

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

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


(E)-Methyl 3-(3-(chlorosulfonyl)phenyl)acrylate is a versatile compound that finds significant application in various chemical synthesis processes. One of its key uses is as a valuable building block in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry and material science.This compound serves as a crucial intermediate for the synthesis of pharmaceuticals, agrochemicals, and functional materials due to its ability to undergo various chemical transformations. Its acrylate functionality allows for efficient cross-coupling reactions, such as Suzuki-Miyaura, Heck, and Sonogashira couplings, enabling the incorporation of diverse functional groups into the final product.In addition, the presence of the chlorosulfonyl group provides a powerful handle for further functionalization through nucleophilic substitution reactions, leading to the creation of a wide range of derivatives with tailored properties. The unique combination of these reactive groups makes (E)-Methyl 3-(3-(chlorosulfonyl)phenyl)acrylate a valuable tool for chemists seeking to design and synthesize novel compounds with specific applications in mind.