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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)-

Propanoic acid, 3-(phenylsulfonyl)-

OC(=O)CCS(=O)(=O)c1ccccc1 Request for Quotation
Chemical Name: Propanoic acid, 3-(phenylsulfonyl)-
CAS Number: 10154-71-9
Product Number: AG0004R9(AGN-PC-0JSTFR)
Synonyms:
MDL No:
Molecular Formula: C9H10O4S
Molecular Weight: 214.2383

Identification/Properties

Properties
MP:
128-130 °C
BP:
458.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Solubility:
methanol: soluble25mg/mL, clear, colorless
Computed Properties
Molecular Weight:
214.235g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
214.03g/mol
Monoisotopic Mass:
214.03g/mol
Topological Polar Surface Area:
79.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
282
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Phenylsulfonyl)propanoic acid is a versatile compound commonly used in chemical synthesis for its unique properties and reactions. It serves as a key building block in the creation of various organic molecules due to its ability to participate in different types of transformations.One prominent application of 3-(Phenylsulfonyl)propanoic acid is in the synthesis of pharmaceutical intermediates. Its presence in drug synthesis allows for the introduction of the sulfonyl group into the desired molecule, imparting specific biological activities or enhancing the overall pharmacological profile of the final product.Furthermore, this compound can be utilized in the preparation of complex molecules in organic chemistry. Its reactivity allows for efficient functional group manipulations, such as coupling reactions, ring formations, and stereochemical control, making it a valuable tool for synthetic chemists aiming to construct intricate molecular structures.In summary, 3-(Phenylsulfonyl)propanoic acid plays a crucial role in chemical synthesis by enabling the construction of diverse organic compounds with tailored properties and functions. Its versatility and reactivity make it an indispensable component in the toolbox of synthetic chemists across various industries.